Nitro

Please enquire for more information about 4-(3-Nitrophenyl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-6-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Methyl-2-propanyl 4-fluoro-3-nitrobenzoate is a synthetic molecule that is used as a model compound for the synthesis of other organic compounds. It has been proposed as a potential treatment for malaria and cancer. 2MP4FNB, as it is often called, can be used to study the conformational and sterochemical properties of molecules. This molecule has also been shown to have anti-inflammatory and antibacterial properties in silico and in vivo experiments.

3,5-Dinitropyridin-4-amine is a synthetic compound that is used as a reagent in organic synthesis. It is also used to produce potassium 4-aminopyridine and pyridine 3,5-dinitrosobenzene. This product has been shown to be a good nucleophile, which can react with fluoride ion or aminopyridine to form an azide. The byproduct of this reaction is an organic acid, which can have detrimental effects on the environment if released. 3,5-Dinitropyridin-4-amine is found in industrial waste and has been shown to have potential environmental pollution when it reacts with nitric acid or sulfuric acid.

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Ethyl 5-[2-Chloro-4-(Trifluoromethyl)Phenoxy]-2-Nitrobenzoate is an active form of retinoic acid, a natural hormone that regulates the growth and development of cells. It is used as a plant growth regulator to induce leaf formation in plants that are not green or chlorophyllous. This product has been shown to be cytotoxic against subtilis, which are Gram-positive bacteria that are not affected by other antibiotics. Ethyl 5-[2-Chloro-4-(Trifluoromethyl)Phenoxy]-2-Nitrobenzoate has also been found to inhibit nuclear DNA synthesis and fatty acid synthesis in plants.

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(5-Methyl-2-nitrophenyl)methanol is a cinnamyl alcohol and a natural antioxidant. It is an inorganic compound that can be synthesized from pyridine and formaldehyde. The compound is used to produce 2-nitrobenzaldehyde, which can be reacted with methacrylates such as methyl methacrylate to produce polymers. This compound has been used in the synthesis of imidazole derivatives, yielding yields of up to 95%.

1-(Mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole is a derivative of aziridine, which is an organic compound with the formula (CH)N=C(CH)NH. It is a white solid that is soluble in water and some organic solvents. 1-(Mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole has been shown to inhibit cancer cell growth in culture by inducing apoptosis and inhibiting the production of reactive oxygen species. This derivative also inhibits the transfer reactions between nitro groups and hydroxyl groups within proteins. This prevents the formation of heterostructures that stabilize proteins in a particular conformational state, leading to their degradation. The amino function on this derivative can be used to modify proteins or other molecules through covalent bonds or other interactions.

Furfural is a molecule with a spectrum that includes the frequencies at which it deforms. The deformation of the molecule can be seen in its nucleus and in the nitrate group. Furfural is an experimental compound that has yet to be studied in depth. It has been found to have three isomers, two of which are shown in this molecule. Furfural's nmr spectra have been measured and it has a molecular weight of 119.18 g/mol.

2-(4-Nitrophenyl)propionic acid is a chiral auxiliary used in organic chemistry to generate enantiomers. It is a methoxy-substituted fatty acid that has been used as an analog of the drug deprenyl, which is an antidepressant. 2-(4-Nitrophenyl)propionic acid has been shown to be effective against estrogen receptor modulators and dopamine reuptake inhibitors. This compound also binds to cannabinoid receptors and fluorescent derivatives have been synthesized for use in kinetic studies.

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4-Chloro-3-nitrobenzanilide is a versatile building block for the preparation of complex compounds. It is used as a reagent in research and as a speciality chemical for the production of high quality fine chemicals. This compound can be used as a reaction component or scaffold to synthesize other compounds. 4-Chloro-3-nitrobenzanilide is a useful intermediate in organic synthesis because it has many functional groups that are easy to modify, making it easy to synthesize new compounds.

4,5-Dimethoxy-2-nitrobenzyl alcohol is a tetrahydrofuran that has photochemical properties. It reacts with uv irradiation to form a hydrodynamic diameter of 6 nm, which is the size of many viruses. The compound can be used as a contrast agent for light microscopy and electron microscopy, or it can be used as a proton donor in organic synthesis. 4,5-Dimethoxy-2-nitrobenzyl alcohol is also used in the laboratory for patterning surfaces by refluxing and expressed as an acid chloride. This product has been shown to react with chloride ions under irradiation to form 6-nitropiperonyl alcohol, which is a molecule that absorbs light at 300 nm and fluoresces at 430 nm. This compound can be cleaved from its substrate by light exposure, making it possible to use this product in photocleavable reactions.

Methyl 3-bromo-5-nitrobenzoate is a solvent that has been shown to interact with centrosymmetric molecules. It crystallizes as a crystalline form and can be synthesized in the presence of heterotopic substituents. Methyl 3-bromo-5-nitrobenzoate can be used as a solvent for cyclic compounds and forms a crystalline conformation in the presence of protonated substituents. This compound is multifunctional, as it can also be used as an insecticide and dye.

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2-Methyl-5-nitropyridin-3-amine is a heterocyclic compound that is synthesized by the cyclization of 2-methylpyridine with sodium nitrite. The reaction product is hydrolyzed to yield the desired compound, 5-nitropyridine. The synthesis of this compound can be used as a target for organic synthesis.

1,2-Diethoxy-4-nitrobenzene is a chemical compound with the formula CH2O2C6H4NO2. It is a colorless liquid that reacts with malonate to produce diethyl malonate and glycol. The reaction has been shown to be optimal at pH = 1.8 when using bromoethane as a solvent. The crystal structure of 1,2-diethoxy-4-nitrobenzene has been determined by X-ray crystallography and it was found to have a monoclinic space group P21/c with cell dimensions of a = 17.928(3) Å, b = 8.096(1) Å, c = 12.547(1) Å and β = 112.38(1)°. The reaction was performed in methylene chloride under phase transfer conditions at 25 °C for 2 hours on average

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Please enquire for more information about (2-Butyl-5-nitro-3-benzofuranyl)[4-[3-(dibutylamino)propoxy]phenyl]methanoneHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Iniparib is a cancer drug that belongs to the class of platinum-based chemotherapy drugs. It inhibits the activity of pro-apoptotic proteins and is used to treat ovarian cancer with low potency. Iniparib has been shown to inhibit the growth of breast cancer cells, as well as other types of cancers. The drug also has an inhibiting effect on metabolic disorders, such as obesity and diabetes, which may be linked to its homologous properties. Iniparib may be useful in treating certain cancers because it has minimal toxicity levels and a low potential for systemic side effects that are common with other chemotherapeutic agents.END>

4,4'-Dinitro-2,2'-bipyridine-N,N'-dioxide is a fine chemical with a high quality. It is a versatile building block with a wide range of applications in research and as a reagent. The compound is used in the synthesis of organic compounds and many other products. This product can be used as an intermediate for the production of more complex compounds or scaffolds. 4,4'-Dinitro-2,2'-bipyridine-N,N'-dioxide has been shown to be useful in the synthesis of pharmaceuticals and agrochemicals.

Please enquire for more information about 4-[4-Nitro-2-(trifluoromethyl)phenyl]morpholine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Nitro-phenyl)-di-p-tolyl-amine is a planar, functionalized molecule that is used as an electron acceptor in dye-sensitized solar cells. A typical dye sensitizer is a porphyrin compound that absorbs light and then transfers the energy to the electron acceptor. The electron acceptor, 4-nitro-phenyl)-di-p-tolyl-amine, accepts electrons and transports them to the electrode where they are reduced to form hydrogen gas. This process generates a photocurrent which can be used as an electrical current. The efficiency of this material is dependent on its density and coefficients, which have been measured at 1.03 cm3/molecule and 0.33 eV per molecule, respectively.

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Please enquire for more information about 1-(2-Chloro-5-nitrobenzoyl)pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4,4'-Dinitrodiphenylmethane is a synthetic chemical that has the formula CHClNO. It is an intermediate in the synthesis of other chemicals. 4,4'-Dinitrodiphenylmethane can be prepared by treating hydrochloric acid with tetraethylammonium chloride and sodium perchlorate. The compound is a white solid that is soluble in water. The molecular weight of 4,4'-dinitrodiphenylmethane is 186.9 g/mol and its molecular formula is C6H5ClN2O. This compound has been shown to have protonation and kinetic constants of 9.2 x 10-11 mol/L and 8.7 x 10-8 cm3/molecule sec respectively. It also has a pKa value of 3.96 at 25 degrees Celsius which indicates that it is more acidic than benzoic acid (pKa=4). This chemical has been

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1-(5-Nitropyridin-2-yl)piperazine is an antibacterial agent with a broad spectrum of activity. It is active against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), and Gram-negative bacteria, such as Pseudomonas aeruginosa. 1-(5-Nitropyridin-2-yl)piperazine inhibits the growth of bacteria by inhibiting bacterial DNA synthesis. The inhibitory concentration varies among different types of bacteria and ranges from 0.03 μg/mL to 10 μg/mL. This drug has been shown to be effective against oxazolidinones, epidermidis, and insecticidal activities in the moth P. xylostella.

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2-Bromo-5-cyanonitrobenzene is a chemical compound that has been shown to have broad-spectrum activity against drug-resistant bacteria. It is able to kill gram-negative and gram-positive bacteria, including drug-resistant strains. The mechanism of action for 2-bromo-5-cyanonitrobenzene is not well understood but it has been observed that the molecule undergoes an oxidative cyclization reaction in the presence of chloride ions or hydroxides. This process leads to the formation of a nitrosobenzene metabolite which reacts with DNA to inhibit protein synthesis and cause cell death. 2-Bromo-5-cyanonitrobenzene has also been shown to be potent against a wide range of different types of bacteria, including those most commonly associated with skin infections, respiratory tract infections, and urinary tract infections.

N,N-Dimethyl-2,4-dinitroaniline is a monomer that belongs to the group of dinitroanilines. It is a colorless liquid with an odorless or faint odor and is soluble in water. N,N-Dimethyl-2,4-dinitroaniline can be used as an emulsifier in cosmetics. The chemical also has potential use as a thermodynamic transfer agent for styrene and as a spectrum enhancer for benzene and sulfate.

Please enquire for more information about 4-Nitro-D-phenylalanine ethylester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Methoxy-3-nitropyridine is a chemical compound with the molecular formula CHNO. It is classified as an amine and has a molecular weight of 140.24 g/mol. 2-Methoxy-3-nitropyridine is a colorless liquid that can be used to make other compounds, such as nitroarenes, boronic acids, and dyes. The molecule consists of a central carbon atom with four nitrogen atoms at the corners of a tetrahedron. The electron configuration for this molecule is 1s22s22p4. This means that the outer shell electrons are in orbitals with principal quantum numbers s=1 and p=2. These orbitals are located near the middle of the molecule rather than on the periphery as in ethane (CH3CH2). This orientation provides more space for other atoms to attach to the central carbon atom, which increases its affinity for nucleophilic attack. 2-M

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4-Methoxy-4'-nitrostilbene is an aromatic compound that appears as a yellow solid. It is used in the synthesis of other compounds, such as chloride and acetonitrile. The epoxidation of this molecule is the first step in a two-step process to make an olefinic compound. This reaction is accomplished with hydrogen peroxide as the oxidant and iodosobenzene as the stabilizer. The second step involves a stepwise addition of chlorine to the epoxide intermediate to form an olefinic product. 4-Methoxy-4'-nitrostilbene can be used as a fluorescent dye for optical analysis or it can be used to provide solvents for other reactions.

1-(2-Iodoethyl)-2-methyl-5-nitro-1H-imidazole (IEMN) is a nitroimidazole that binds to lipid nanoparticles. IEMN interacts with the blood vessel wall and inhibits cancer cell growth by inhibiting the synthesis of lipids. It has been shown to be a potent anti-cancer drug for use in diagnostic imaging, as well as in treating solid cancers. IEMN also has cytotoxic effects on cancer cells, which may be due to its ability to inhibit the production of proteins required for cell division.

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3-Nitrobenzenesulfonohydrazide is a potent inhibitor of α-amylase. It is an equated inhibitor that can be used in a molecular docking study to predict the interaction between α-amylase and 3-nitrobenzenesulfonohydrazide. This inhibitor has been shown to have a strong inhibitory potential against α-amylase and it may be useful for the treatment of type 2 diabetes mellitus. 3-Nitrobenzenesulfonohydrazide also has been shown to have inhibitory effects on other enzymes, such as β-glucosidase, which can be used in the treatment of disorders related to carbohydrate metabolism. 3NBSH is also a spectroscopic technique that has been used to study the interactions between this compound and various proteins.

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2,4-Dinitro-5-methylphenylhydrazine (DMN) is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used to synthesize high quality reagents and reaction components for research purposes. DMN has been shown to have a number of properties that make it useful in industrial processes, including its stability and resistance to heat and light.

Nicarbazin is a nitrofuran that is used as a feed additive in animal feeds. It is also used to prevent or treat coccidiosis, an intestinal disease caused by the protozoan parasite Eimeria tenella, in chickens and turkeys. Nicarbazin inhibits growth of coccidia oocysts (eggs) and prevents oocyst production in the intestine. The drug has been shown to have no significant effect on the antigenicity of either nicarbazin or its metabolites when administered with a human food antigen. Nicarbazin also has been shown to be safe for animals such as dogs, cats, and horses at dosages up to 100 mg per kg body weight per day for periods of up to six months. Nicarbazin's mechanism of action involves binding to the nicotinamide adenine dinucleotide-bound form of nicotinamide adenine dinucleotide phosphate-reducing enzyme (NADPH-

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2,6-Difluoro-3-nitropyridine is a synthetic chemical compound that is used as a reagent in the synthesis of other compounds. It is also used to synthesize esters and nucleophilic compounds. 2,6-Difluoro-3-nitropyridine has been shown to react with ethoxymethylene malonate, morpholine and acidic ethanolates to form esters. This compound reacts with sulfoxide to form sulfones. The chemistry of this compound has been investigated by reacting it with fluoride in an acidic solution. It can also be hydrolyzed by water or alkali to form 2,6-difluoropyridine.

5-Chloro-2-nitrocinnamic acid is a fine chemical with a CAS number of 20357-28-2. It is a versatile building block that can be used as a reaction component or intermediate in the synthesis of more complex compounds. The high purity and quality of 5-Chloro-2-nitrocinnamic acid makes it an ideal reagent for research purposes, and it can be used as a building block for the synthesis of useful scaffolds.

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4-Chloro-2-fluoro-5-nitroaniline is a fine chemical that is used as a reagent and speciality chemical in research, as well as a building block for the synthesis of complex compounds. 4-Chloro-2-fluoro-5-nitroaniline has been shown to be an excellent building block for the synthesis of versatile scaffolds, which can be used in the production of drugs with antibacterial properties. This product is also useful as a reaction component for the synthesis of high quality, complex compounds.

Please enquire for more information about N,N-Dipropyl-2-methyl-3-nitrophenylethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Isonitrosopropiophenone is a proximal tubule toxicant that inhibits the activity of copper, which is essential for protein synthesis. It is a potential optical sensor in diagnostic testing and has been shown to be an optimal reactant with optical sensors. 2-Isonitrosopropiophenone has been shown to form a complex with copper ions, which are necessary for the oxidation of sulfonic acids. The reaction mechanism involves the formation of hydrogen chloride, which reacts with hydrochloric acid to produce hydrochloric acid and water. This reaction proceeds by way of intermolecular hydrogen bonding between reactive groups on the 2-Isonitrosopropiophenone molecule and reactive sites on the copper ion.

2-(4-Nitrobenzyl)pyridine is a nucleoside that contains an amino group. It has been shown to be able to be converted into 2'-deoxycytidine and 2'-deoxyadenosine, two nucleosides that are used in the synthesis of acyclic nucleosides. The conversion of 2-(4-nitrobenzyl)pyridine to these nucleosides occurs by the action of sulfites, which convert the nitro group to an amine. This reaction can also take place in the presence of sodium hydroxide or zinc chloride. The sequence of the molecule can be found using a number of techniques, including dioxane and cidofovir. 2-(4-Nitrobenzyl)pyridine is also used in the production of cyclopropylamine, which is a drug used for the treatment of HIV infection.

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Applications 3,5-DINITRO-4-HYDROXYBENZOIC ACID (cas# 1019-52-9) is a useful research chemical.

1,1'-[Ethane-1,2-diylbis(oxy)]bis(4-nitrobenzene) is an ether with a nitro group. It is used in the production of glycols and as a solvent for dyes and other organic compounds. This compound is also used in catalytic reactions, such as hydration of ethylene oxide to produce ethylene glycol. It is an intermediate in the synthesis of 1,2-ethanediol from sodium nitrite and formaldehyde. The hydrolysis of 1,1'-[ethane-1,2-diylbis(oxy)]bis(4-nitrobenzene) yields 4-(hydroxymethyl)phenol and 2-(nitrosomethyl)tetrahydrofuran. Hydrolysis at elevated temperatures produces 4-(hydroxymethyl)-3-nitrophenol, which undergoes further reactions to form 3-[2-(tr

4-Nitropyridine is a nitro compound that has been synthesized according to the quantum theory of molecular structure. It is a molecule with the empirical formula C6H4N2O2, consisting of a central carbon atom with four nitrogen atoms in an octahedral arrangement around it. The molecule can be protonated and deprotonated, resulting in an n-oxide form or as a dipole. 4-Nitropyridine has optical properties that make it suitable for use as an indicator dye. This compound also forms hydrogen bonds with other molecules and can form strong complexes with metal ions such as sodium carbonate and hydrochloric acid. 4-Nitropyridine's frequency shifts are dependent on the solvent conditions.

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5-Chloro-2-nitrophenylhydrazine (5CNP) is a reactive, chlorine-containing molecule that has been shown to form covalent bonds. It is an amine with a chlorine atom in the 5th position. The molecular modeling study of 5CNP showed that it can act as a nucleophile and react with an electron-deficient acceptor to form a cyclic intermediate. This reaction can be induced by activating the phenyl hydrazine through electrophilic substitution or cyclodehydration, which produces an alicyclic intermediate with two adjacent chlorine atoms.

3-Nitro-1,2,4-triazole is a heterocyclic compound that can be used in organic synthesis. It has been shown to react with nucleophiles such as thiols and amines. The reaction products are covalent adducts, which are low detection and can be used for the chemical analysis of nucleophiles. 3-Nitro-1,2,4-triazole is also known to form a coordination complex with palladium (II) chloride and zinc chloride in the presence of a base. This coordination complex has been shown to inhibit the growth of v79 cells in vitro. 3-Nitro-1,2,4-triazole has also been shown to have antiangiogenic properties and inhibit tumor growth in animal models.

3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine is a chemical compound that can be used as a reaction component or reagent in research. It is a useful scaffold and building block for complex compounds. 3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine has CAS No. 2078-01-5 and is classified as a speciality chemical. This chemical is versatile because it has many uses in both organic chemistry and biology, including use as an intermediate or building block for more complex compounds.

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3-(Methylnitrosamino)propionitrile (NNK) is a potent, but toxic, carcinogen that has been shown to be one of the major causes of lung cancer in animals. It is metabolized to 3-aminobenzamide and N-nitrosodimethylamine (NDMA) by cytochrome P450 enzymes. These metabolites are then further converted into reactive species that bind covalently with DNA, leading to mutations and ultimately cancer. The activation of NNK can be prevented by inhibiting the enzyme hydrolysis or by blocking the synthesis of the reactive metabolites.

4-(3-Nitrophenyl)-1,3-thiazol-2-amine is a spectroscopically active compound that has been reported to have a melting point of about 190°C. It has an absorption maximum of 208 nm and is soluble in acetone, benzene, chloroform, ether, methanol, and water. The yield for the reaction was determined to be about 63%. The chemical structure consists of a thiazole ring with two nitro groups on the phenyl ring. 4-(3-Nitrophenyl)-1,3-thiazol-2-amine has also been shown to react with amines to form oxychlorides. Citric acid can also be used as a reagent for this process.