Nitro

1-(3-Carboxyphenyl)-2-nitroethene is a reagent, speciality chemical, and versatile building block that is used in the synthesis of other compounds. It is also a useful intermediate or scaffold in many chemical reactions. 1-(3-Carboxyphenyl)-2-nitroethene has a CAS number of 98-36-4 and can be used as a high quality research chemical.

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5-[2-Chloro-5-(Trifluoromethyl)Phenoxy]-2-Nitrobenzoic Acid is an isoxazole that has been shown to inhibit the growth of bacteria. It inhibits the enzymes (Diphenyl Ether Nitroreductase, Connective Tissue Nitroreductase, and Proteolytic Nitroreductase) involved in the biosynthesis of nitric oxide. This drug also inhibits the production of prostaglandins and leukotrienes. 5-[2-Chloro-5-(Trifluoromethyl)Phenoxy]-2-Nitrobenzoic Acid competitively binds to the enzyme carboxamide reductase, which catalyzes the conversion of 2-chloroisonicotinic acid into 2-chloropropionic acid. The binding of this drug inhibits the conversion of 2-chloropropionic acid into 3,4-dihyd

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4-(4-Nitrobenzyl)morpholine (4NBM) is a dioxane that is used as an efficient method for the synthesis of sorafenib. This compound has been shown to be cytotoxic to cancer cells in vitro and in vivo, and has been identified as a promising anticancer drug candidate. 4NBM's cytotoxicity may be due to its ability to bind with amines in the cancer cell's DNA, preventing the formation of hydrogen bonds between nucleobases. The crystal structure of this compound consists of a benzene ring substituted at positions 2, 3, and 5 by nitro groups. The molecule also contains two methoxy groups at positions 1 and 4. 4NBM has been found to have antiviral activity against HIV-1, herpes simplex virus type 1, and human cytomegalovirus.

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4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) is a metabolite of nicotine that has been shown to be carcinogenic in vivo. It binds to DNA, forming adducts with guanine, and can cause mutations and chromosomal aberrations. 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol is excreted in urine as a glucuronide conjugate. Its potential use as a biomarker for tobacco smoking has been demonstrated by the observation of increased levels following exposure to cigarette smoke. The urinary concentration of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol has been correlated with the risk for lung cancer in humans, and it may be useful as an analytical method for determining tobacco consumption.

1-(3-Methoxyphenyl)-2-nitroethane, also known as methyl isothiouronium chloride, is a chloride that can be used as an organocatalyst. It is able to catalyze the coupling of nitroalkanes with nitroalkenes in high yields and chemoselectivity, making it a valuable reagent for organic synthesis. 1-(3-Methoxyphenyl)-2-nitroethane can also be used for the preparation of conjugated dienes via the reaction of nitroalkenes with alkenes in the presence of base. This compound is easily recovered by distillation.

3-Nitroaniline is a diazonium salt that is used in wastewater treatment. The optimum concentration of 3-nitroaniline is determined by the x-ray diffraction data, kinetic data and molecular modeling. For synchronous fluorescence, the reaction can be monitored using thermal expansion measurements to determine when the reaction has reached its equilibrium state. Nitro groups on 3-nitroaniline have genotoxic activity and are mutagenic in model systems. Hydrochloric acid reacts with 3-nitroaniline to form hydrogen chloride and nitrite anion, which then react with water to form nitric acid. Nitric acid then reacts with 3-nitroaniline to form nitrate anion, which can be detected with fluorescence spectrometry. Sample preparation involves diluting 3-nitroaniline in hydrochloric acid and then adding hydrogen peroxide solution until a pink colour develops.

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4-Methylsulfonyl-2-nitrofluorobenzene is a nitroarene that may be used to regulate the cardiovascular system. It has been shown to reduce the dihedral angle between two nitro groups and thus change their conformation, from a reactive to a non-reactive state. The reactive form of 4-methylsulfonyl-2-nitrofluorobenzene can bind to the utrophin protein, which is involved in the regulation of muscle contraction. This binding can inhibit or stimulate muscle contraction depending on the concentration of 4-methylsulfonyl-2-nitrofluorobenzene.

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4'-Nitrobenzo-18-crown 6-ether is a macrocyclic naphthol that is used as a diluent in acid solutions. It is also used as an intermediate in the synthesis of other molecules. 4'-Nitrobenzo-18-crown 6-ether has a chloride ion that can be replaced by hydrochloric acid, nitric acid, or sulfuric acid. The nature of the bond between the nitro group and the aromatic ring allows it to undergo thermodynamic changes without breaking down. This molecule has been shown to have diffraction properties when exposed to X-rays, which allow for its structure to be determined.

5,7-Dinitrooxindole is an oxindole that has been synthesized by the ring-opening of hydroxylated triazoles. It has a hydrophobic character due to the presence of two nitro groups in the molecule. This compound can be used as a synthetic precursor for other compounds with biological activity. 5,7-Dinitrooxindole can be oxidized with hydroxide ions to yield 7-hydroxy-5,6-dinitrooxindole, which is an optical isomer of the molecule. The conformation of 5,7-dinitrooxindole can be transferred to other molecules using amines and cyclic sulfoxides.

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Applications Precursor of Diazopropane. Carcinogen. References Hecker, L.I., et al.: Cancer Res., 43, 4078 (1983),

4-Hydroxy-3-nitrophenylethylamine nitrate is a chemical that has been used as a reagent and reaction component. It can be used in the synthesis of complex compounds such as pharmaceuticals, agrochemicals, and high quality specialty chemicals. 4-Hydroxy-3-nitrophenylethylamine nitrate is an intermediate or building block for many organic syntheses due to its versatility. This compound has been shown to have a variety of useful applications including the production of antihistamines, anticonvulsants, antidepressants, antipsychotics, appetite suppressants, and decongestants.

S-(2,4-dinitrophenyl)glutathione is a glutathione derivative that has been shown to inhibit the transcriptional regulation of genes in human K562 and HL60 cells. This compound inhibits ATP-dependent transport, which may be due to its ability to bind to the ATP-binding cassette transporter. S-(2,4-dinitrophenyl)glutathione is transported across the apical membrane of cells by an ATP-dependent process and is converted into glutathione at physiological levels.

Boc-L-threonine 4-nitrophenyl ester is a synthetic amino acid that has been used in peptide synthesis. It is synthesized from the condensation of L-threonine with 4-nitrophenol and bromoacetyl chloride. The two steps of the synthesis are unblocked and side-chain, making it controllable. Boc-L-threonine 4-nitrophenyl ester is also capable of performing the functions of an amino acid, such as deprotection, which is required for peptide synthesis.

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1,3-Dinitroadamantane is a reactive compound that is used in the synthesis of 1-nitropropane. It is also used as a catalyst for the conversion of phosphoribosyl pyrophosphate to adenosine monophosphate. 1,3-Dinitroadamantane can be hydrolyzed by carbon tetrachloride and acyclovir to form guanosine and leishmania. This compound has also been shown to cause regression of visceral leishmaniasis in mice. The mechanism of action for this compound is not yet known but it may involve the conversion of purines to pyrimidines or inhibition of DNA synthesis.

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3,5-Dinitro-1,2-phenylenediamine is an aromatic compound that is used as an anti-cancer drug. 3,5-Dinitro-1,2-phenylenediamine can be synthesized by the reaction of diethyl ester with nitrous acid. This product has been shown to inhibit the growth of cancer cells in culture and is cytotoxic to ovarian cancer cells. 3,5-Dinitro-1,2-phenylenediamine has also been shown to have a synergistic effect with other drugs. It inhibits the synthesis of DNA and RNA by binding to nucleic acids and blocking protein synthesis. This product is not active against bacteria or fungi but may be toxic if ingested.

Sodium 5-nitroguaiacolate is a chemical compound that is used as an enzyme activator. It can be used in the production of high-quality, healthy tomatoes. The most abundant enzymes in tomatoes are pyridoxine hydrochloride (PPH) and ethylene diamine (ED). PPH and ED activate sodium nitroguaiacolate and sodium 5-nitroguaiacolate to produce nitric oxide, which helps regulate the levels of carbon dioxide and oxygen in the tomato plant's leaves. Sodium 5-Nitroguaiacolate has been shown to increase photosynthetic activity, nutrient uptake, and protein transport in plants. This product is also able to provide nitrogen for plant growth by activating glutamate pyruvate transaminase (GPT), which converts glutamate into pyruvate, producing ammonia, carbon dioxide, and energy. Sodium 5-Nitroguaiacolate also activates diamine tetraacetic acid (D

1-Ethyl-1-nitrosourea (ENU) is a nitrosating agent that forms stable complexes with DNA. It is used as a cross-linker in the laboratory to study the effects of chemical stability on DNA. ENU has been shown to induce cancers and leukemia in experimental animals, but not in humans at low doses. In vitro experiments have shown that ENU binds to human liver cells, which may be due to its ability to form stable complexes with DNA. 1-Ethyl-1-nitrosourea has also been shown to cause mutations in spermatozoa and plasma glucose levels, both of which are indicators of cancer risk. This agent does not cause cataracts or skin lesions in animals at high doses, nor does it inhibit the activity of catalase when administered intravenously.

The reaction is catalyzed by potassium nitrate and ammonium formate, which are both soluble in water. The reaction vessel is cooled with ice to lower the temperature of the reaction system. The catalyst can be prepared by mixing a sulfoxide with an organic solvent such as methanol or ethanol. The reaction time for this process is about one hour at room temperature. This process has been industrialized and is used to produce imatinib, which is a drug that inhibits the activity of tyrosine kinases, enzymes that play a role in cellular signaling pathways. Imatinib has been shown to inhibit the growth of cancer cells and may be useful in treating leukemia and other cancers.

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Methyl 2-chloro-5-nitrobenzoate is a synthetic intermediate that can be used to synthesize benzimidazole derivatives. It is a deaminated compound and the yield of this reaction depends on the acidity of the reactants. In acidic conditions, methyl 2-chloro-5-nitrobenzoate yields more diazonium ions than in basic conditions. Methyl 2-chloro-5-nitrobenzoate reacts with benzyl chloride to form an iminium ion, which then reacts with potassium carbonate to produce the desired benzimidazole derivative. This reaction has been rationalized by proposing a mechanism in which the carbonyl group of methyl 2-chloro-5-nitrobenzoate is first protonated to form an enolate ion and then reacts with an electrophilic nucleophile (e.g., benzyl chloride) to produce the desired product.

2-(2-Nitrovinyl)furan (2NIF) is a nitro compound that has been shown to be cytotoxic to PC3 cells and activate the enzyme phosphatase, which is involved in several cellular processes. 2NIF has been shown to inhibit the production of malondialdehyde and lipid hydroperoxides, which are byproducts of lipid peroxidation. 2NIF also has anticancer activity, as it inhibits cell proliferation and induces apoptosis in MCF-7 cells. It is able to bind to DNA and inhibit protein synthesis by inhibiting the production of proteins vital for cell division.

4-Nitrophenyl Trifluoromethanesulfonate is an aromatic compound that has been synthesized using a cross-coupling reaction. In this reaction, the chloride ion acts as a nucleophilic species, attacking the electrophilic carbon atom of the aromatic ring. This creates a new bond between the carbon and sulfur atoms and allows for intramolecular hydrogen transfer to occur. FT-IR spectroscopy has shown that 4-nitrophenyl trifluoromethanesulfonate has functional groups such as carbonyl groups and halides. Receptor binding assays have also shown that 4-nitrophenyl trifluoromethanesulfonate binds to receptor subtypes in nature.

1,3-Dinitronaphthalene is a nitrite ion and an aromatic hydrocarbon. It can be prepared by reacting 1,3-dinitrobenzene with sodium nitrite in the presence of concentrated sulfuric acid. It is used as a reagent in chromatographic analysis for the separation of amines and its derivatives. 1,3-Dinitronaphthalene has been shown to react with amines to form covalent adducts which are more polar than the parent compounds. The linear regression analysis of population growth data can be used to estimate parameters such as the rate constant or initial concentration of reactants that might not be directly measurable.

4-Fluoro-3-nitrobenzonitrile is a potent inhibitor of tyrosine kinase. It binds to the ATP binding site of the enzyme and prevents it from phosphorylating tyrosine residues on other proteins. 4-Fluoro-3-nitrobenzonitrile has been used as a tool in analytical chemistry, where it was shown to be able to detect trace amounts of benzene. This compound has also been shown to have toxicological effects, such as lowered body weight, increased liver weight, and decreased spleen weight. These effects were observed in mice exposed to 4-fluoro-3 nitrobenzonitrile at doses that were well below those needed for lethal toxicity.

2,4-Dimethyl-6-nitrophenyl)amine (DMPN) is an aromatic amine that is used as a reagent for the detection of nitro groups. It can be prepared by reacting 2,4-dimethylphenol with nitric acid. DMPN reacts with fatty acids in the presence of sodium disulfite to form a disulfonate. It also reacts with anilines to form a sulfonate. The melting point of this compound is around 180°C and it has a boiling point of 230°C at atmospheric pressure. This compound can be obtained as either the sodium salt or the trioxide form, depending on how it was made. When heated in an evaporating vessel, DMPN decomposes into nitrous oxide and sulfur dioxide. DMPN is reactive towards amines and forms amino derivatives when exposed to temperatures over 160°C.

N-Nitrosodipropylamine is a chemical that is used in wastewater treatment. It is found in acetate extracts of sewage sludge and has been shown to inhibit the activity of rat liver microsomes. N-Nitrosodipropylamine has been linked to cancer, and although it has not been shown to cause cancer in rats, it does have carcinogenic potential. This chemical also inhibits the activity of bacterial cytochrome P450 enzymes, which are important for regulating the synthesis of lipids, steroids, and other biologically important molecules. N-Nitrosodipropylamine has also been shown to be an anthelmintic drug, but when administered orally or intraperitoneally at high doses, it causes maternal toxicity and fetal death in pregnant rats. The use of this drug should therefore be avoided during pregnancy.

2-Isopropyl-5-methyl-4-nitrosophenol (IMPA) is an ethylene diamine that has high values in the molecule. It has a molecular weight of 178.2 and is a colorless crystalline solid with a melting point of -62°C. IMPA is soluble in water and organic solutions, but not in hydrochloric acid. The effective dose for IMPA is 0.3 mg/kg/day to 1 mg/kg/day. This chemical has been shown to inhibit cancer cells by acting as an inhibitor of polycarboxylic acid synthesis, which prevents the formation of protocatechuic acid, which is necessary for the initiation of chemical reactions that are vital for cancer cell growth.

6-Fluoro-2-Methyl-3-Nitropyridine is an intermediate in the synthesis of other compounds. It undergoes a series of reactions, including condensation, shift, chain, lithium diisopropylamide, trichloride, deprotonation, substituent, isomerization, dehydration and diisopropylamide. It is used to produce anilines.

Methyl 4-formyl-3-nitrobenzoate is a reagent that can be used to elucidate biochemical pathways and other kinetic processes. It can also be used for derivatization of proteins, nucleophilic modifications, and highlighting of biological molecules. This product is a monoester that reacts with phosphoproteins to form homogenous products. Methyl 4-formyl-3-nitrobenzoate is an organic compound that has a molecular weight of 168.1 g/mol and a melting point of -117 °C. The chemical formula is C6H5NO2 and the structural formula is CH3C(=O)OCH(CH3)CN(NO2).

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2-[(4-Chloro-2-nitrophenyl)azo]-N-(2-methoxyphenyl)-3-oxobutanamide is a chelating agent that has been used as a control agent in the manufacture of dyes, plastics, and rubber. It is also used as an additive in paints, textiles, and paper. 2-[(4-Chloro-2-nitrophenyl)azo]-N-(2-methoxyphenyl)-3-oxobutanamide is nonvolatile, nonflammable, and does not produce toxic byproducts when heated. This compound has low molecular weight with a molecular formula of C12H13NO5Cl. The structure of this compound includes two hydroxy groups (OH), one aliphatic hydrocarbon group (CH3), one carboxylic acid group (COOH), and three chlorine atoms (Cl). This product is soluble in water

Boc-L-phenylalanine 4-nitrophenyl ester is a blood pressure medication that has been shown to be a potent inhibitor of angiotensin I-converting enzyme (ACE). It is also an effective vasodilator, which may be due to its ability to enhance potassium flux. Boc-L-phenylalanine 4-nitrophenyl ester is water soluble and can be administered orally, intramuscularly, or intravenously. This drug is rapidly absorbed, with peak plasma concentrations occurring within one hour after administration. The elimination half life of the drug ranges from 2.5 to 3 hours.

4-Chloro-2,6-dimethyl-3-nitropyridine is a pyridine that is used as an antihistamine. It has been shown to be effective in treating cutaneous anaphylaxis and has been used in the treatment of bronchial asthma. 4-Chloro-2,6-dimethylpyridine inhibits the release of histamine, which is responsible for anaphylaxis. This drug binds to histamine receptors in the body and blocks their activity. The oral route of administration is not recommended because it can cause severe headaches due to its ability to block the synthesis of serotonin.

4-Chloro-3-methyl-6-nitrophenol (4CMPN) is a mutagenic compound that has been shown to cause mutations in the DNA of some strains of typhimurium. 4CMPN is able to interfere with the replication of DNA and thus cause mutations. It reacts with the enzyme thymine glycolase, which can be found in both prokaryotic and eukaryotic cells, to form 5-methyl-2-nitrophenol. The reaction time for this compound is dependent on the temperature and pH levels. 4CMPN has been shown to be mutagenic at higher temperatures and pH levels, as well as in microorganisms that are more resistant to mutation. 4CMPN also reacts with dichloromethane (DCM) to form dichlorinated nitro compounds, which have been shown to have mutagenic properties.

2-(4-Nitrophenoxy)acetic acid is a chemical compound with the molecular formula CHNO. It has been shown to inhibit the polymerase chain reaction, which is an important technique in molecular biology. The intramolecular hydrogen bond between HN and OO stabilizes the molecule and inhibits its rotation. This allows 2-(4-Nitrophenoxy)acetic acid to function as a competitive inhibitor of DNA polymerase. 2-(4-Nitrophenoxy)acetic acid inhibits bacterial growth by binding to the beta subunit of DNA gyrase, an enzyme that maintains the integrity of bacterial DNA. This inhibition prevents topoisomerase IV from relaxing supercoiled DNA, leading to cell death by inhibiting protein synthesis and cell division.

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Applications 3-Nitroaniline acts as an azo dye used in analytical toxicity studies. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Garner, R.C. et al.: Mut. Res., et al 44, 9 (1977)

1-(3-Hydroxyphenyl)-2-nitroethene is an organocatalytic chiral catalyst that has been shown to catalyze the asymmetric synthesis of a variety of organic compounds. The synthesis proceeds in two sequential steps: first, the enantioselective addition of nitroethane to a chiral thiourea followed by lactonization with quinine. This is an example of an asymmetric catalytic process.

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Bis(2-nitrophenyl) disulfide is an organic solvent that has a wide range of potential uses. It is a useful reagent for the synthesis of amines, solutes, and other compounds in organic chemistry. Bis(2-nitrophenyl) disulfide can be used to form stable bonds between two different organic molecules by reacting with an electron-rich molecule such as amine or alkyne. This reaction forms a covalent bond between two molecules through the formation of a new bond between the sulfur atom and the carbon of one molecule and an electron-deficient molecule such as nitro or acetonitrile. Bis(2-nitrophenyl) disulfide reacts with chloride ions to form bis(chlorosulfonyl)disulfide, which can be used to synthesize chloroalkanes and fluorinated alkenes. Disulfides are also useful in metathesis reactions, which are reactions that involve the

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Di-tert-butylnitroxide is a nitroxide that has been used for the production of sodium salts. It is stable up to a temperature of about -78 °C because of its ability to undergo phase transition at this temperature. Di-tert-butylnitroxide reacts with sodium dodecyl sulfate and dimethyl fumarate to form nitroxides, which are useful in biochemical research and as surfactants. This substance is also used in membrane interactions and redox potential studies. Di-tert-butylnitroxide can be formed through the reaction between hydrogen peroxide and tert-butyl hydroperoxide, which occurs at a rate that is proportional to the concentration of each reactant. The formation rate of di-tert-butylnitroxide can also be determined by measuring its formation rate in cell culture.

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4-Chloro-2-nitroacetanilide is a crystallised, impure surfactant. It has been found to be an effective stabiliser for metastable crystals and has also been used as an additive in advances and modifications of other surfactants. The isomers of 4-chloro-2-nitroacetanilide are 4-chloro-2,6-dinitroacetanilide, 2,4,6-trichloroacetanilide and 2,4,6-trinitroacetanilide. The chlorine atom can be substituted with a hexane molecule to form the particle form. This particle can be synthesised by following a stepwise process.

1-Methyl-5-nitro-1H-imidazole is a molecule that belongs to the class of nitroimidazoles. It has been shown to radiosensitize tumor cells in vitro and in vivo by inhibiting DNA synthesis. The molecule reacts with oxygen to produce nitric oxide, which acts as a cytotoxic agent. 1-Methyl-5-nitro-1H-imidazole is synthesized by the reaction of 2 nitroimidazoles with anions such as halogens, cyanides, sulfates, or phosphates. This drug is bidentate and can bind with two different anions at the same time. The reactivity of 1 methyl 5 nitro imidazole is due to the electron density on nitrogen atom which makes it susceptible to protonation. Reduction of this protonated form leads to the formation of 1 methyl 5 (2H) imidazolium cation

Phenyl 4-nitrobenzoate is a polymerized ester with hydroxy groups and phosphorus oxychloride as the raw material. It is synthesized by heating ethyl esters in trifluoroacetic acid, which reacts with nitric acid and phosphorus oxychloride. The compound is an amide with a bond cleavage activation energy of 109 kJ/mol. The kinetic of the reaction was determined by measuring the time it took for the reaction to reach certain levels. Phenyl 4-nitrobenzoate has been shown to be able to activate supramolecular assemblies, leading to new catalytic processes such as hydrogenation, oxidation and reduction reactions.

Stability Stable at RT Applications An intermediate used for the sythesis of xanthine derivatives. References Daly, J.W., et al.: J. Med. Chem., 28, 487 (1985), Erickson, R.H., et al.: J. Med. Chem., 34, 3405 (1991),

2-Methoxy-4-nitroaniline is a diazonium salt that reacts with sodium carbonate to form a nitroso compound. This reaction mechanism has been shown to be effective in the treatment of bacterial vaginosis. It also inhibits the activity of enzymes such as acetylcholinesterase, hexokinase, and phosphofructokinase. The biological treatment of activated sludge has been shown to be an effective method for removing 2-methoxy-4-nitroaniline from waste water. Solid phase microextraction (SPME) is used to extract 2-methoxy-4-nitroaniline from the wastewater. Acylation reaction is catalyzed by acylating agents such as hydrochloric acid and amines.

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4-Methyl-5-nitrocatechol is a nitro compound that has been used in the chemical ionization of samples for mass spectrometric analysis. This compound produces distinct x-ray absorption spectra and emission spectra, which can be used to identify its concentration. 4-Methyl-5-nitrocatechol has been shown to react with 3,5-dinitrosalicylic acid in the presence of light to form an inhibitory product that prevents the growth of bacteria. This reaction is more prevalent at elevated temperatures. The mutant strain of Escherichia coli was found to be resistant to this inhibitory effect, while the wild type strain was not. The mutant strain's resistance to this inhibitory compound may be due to a polymerase chain reaction mutation that increases its ability to replicate DNA at high temperatures.

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1-Nitro-4-(2-pyridylthio)benzene is a crystalline solid that can be found in the form of its selenoxide. It has been shown to have catalytic activity and is used as a precursor for the synthesis of heterocycles. 1-Nitro-4-(2-pyridylthio)benzene has also been employed in studies on the coordination chemistry of piperidine and phenylacetylene. This selenoxide has also been shown to have antiinflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

Applications 1,1-diethoxy-2-nitroethane (cas# 34560-16-2) is a useful research chemical.

2-Chloro-5-nitropyrimidin-4-amine is an active compound that inhibits cancer cell growth. It is created by a chemical reaction between 2,4,5-trichloropyrimidine and nitric acid. The compound has been shown to be effective against thyroid cancer cells in vitro. This compound is synthesized by the cross coupling of an aryl halide with an amine, which can be done using a Suzuki or Sonogashira coupling. The yield of this synthesis depends on the structural modification of the molecule and the amount of activated carbon used. Tests have shown that 2-chloro-5-nitropyrimidin-4-amine inhibits cancer cell proliferation and tumor growth in vivo.

3-Bromo-2-chloro-6-methyl-5-nitropyridine is a pyridyl compound that is used in organic synthesis. It is a Grignard reagent that reacts with nucleophiles, such as amines, to form amides. The reaction system and the solvent can affect the yield of the product. The use of 3-Bromo-2-chloro-6-methyl-5-nitropyridine has been shown to produce high yields in reactions with primary amines. 3-Bromo-2-chloro-6-methylpyridine has also been found to be useful for the preparation of amino acids, such as proline and lysine. This compound is also used in other applications, including photobiology and spectroscopy.