Nitro

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2,4-Dichloro-3,5-dinitrobenzotrifluoride is a chemical compound that is used in an industrial process. It is an inorganic base that reacts with toluidine to form a reaction product. The reaction selectivity of 2,4-Dichloro-3,5-dinitrobenzotrifluoride is constant and the reactions are carried out using an inorganic acid as the solvent. Other impurities may be present after the reaction as byproducts. The reaction time for 2,4-Dichloro-3,5-dinitrobenzotrifluoride is typically about 5 hours. This chemical compound can be used as a pesticide and it has been detected in wastewater from manufacturing plants.

(R,S)-N-Nitroso anatabine is a nitrosamine that is used as an analytical standard for the determination of the covalent binding of carcinogens to DNA. It can be synthesized by reacting (R,S)-N-nitrosodimethylamine with nitric acid in the presence of aluminum chloride. The structure and purity of this compound were confirmed by LC-MS/MS. The compound was found to be carcinogenic when administered to female mice, but not male mice. The carcinogenicity was attributed to the formation of DNA adducts in tissues and the induction of chromosomal aberrations.

3,5-Dinitropyridine is an organic compound that has been shown to be a potent antibiotic against bacteria. 3,5-Dinitropyridine binds to the nucleophilic site on the bacterial cell wall and has been shown to be active against gram-positive and gram-negative bacteria. This drug is activated by hydrogen bonding with water molecules, which triggers a ring opening reaction. The activation energy for this process is 6 kcal/mol. 3,5-Dinitropyridine reacts readily with dimethylformamide (DMF), which acts as the solvent in this reaction. The reaction rate of 3,5-dinitropyridine with DMF was found to be 1.6x10^6 M^3/mole s^1 at 25 degrees Celsius using a constant of 0.1 M/L at pH 7.0 and ionic strength of 0.01 M KCl. It also reacts with copper ions, forming an antibacterial

N-(2,4-Dinitrophenyl)-L-alanine methyl ester (DNPA) is a chemical compound that belongs to the class of nitrophenyl alkyl amides. It is synthesized by reacting 2,4-dinitrobenzene with L-alanine methyl ester and then hydrolyzing the product. DNPA has been used as an analytical reagent in IR spectroscopy due to its high intensity and sensitivity. The electron transfer theory can be used to predict the functional group population of DNPA. An FTIR spectrum was obtained from this molecule which exhibited a strong absorption at 1,640 cm-1 corresponding to the stretching vibration of N--H. This vibrational mode corresponds to the bending vibration of H--N--H, which is in agreement with previous reports on DNPA.

4-Nitro-2-aminophenol-6-sulfonic acid is an organic compound that is a member of the class of sulfonic acids. It has the chemical formula of CHNO, and its molecular weight is 154.11 g/mol. This chemical can be found in the environment as a result of formaldehyde oxidation and salicylic acid decomposition. 4-Nitro-2-aminophenol-6-sulfonic acid has been used in the manufacture of acetoacetates, formaldehydes, and acrylic acids. The reaction between this chemical and potassium sulfate produces diazo, which is then used to produce other chemicals such as sulfanilate or sulfonic group. 4-Nitro-2-aminophenol-6-sulfonic acid has acidic properties that make it useful for complex reactions with salicylic acid. The yellow color comes from its sulfur content, which also makes it corrosive to metals such as

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3'-(Tetrafluoroethoxy)-beta-methyl-beta-nitrostyrene is a versatile building block that can be used as a reaction component for the synthesis of more complex compounds. This compound is also known to have speciality chemical and research chemical properties. 3'-(Tetrafluoroethoxy)-beta-methyl-beta-nitrostyrene has been shown to be an effective reagent for the synthesis of high quality complex compounds.

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5-(4-Nitrophenyl)-1H-tetrazole is a diphenyl sulfoxide compound that can be synthesized using solid-phase synthesis. It has been shown to inhibit the growth of bacteria by acting as an electron donor, which inhibits the activity of bacterial enzymes. 5-(4-Nitrophenyl)-1H-tetrazole has a chloride anion that binds to the active site of the enzyme and reacts with a chloride ion present in the enzyme's environment, forming a complex that is stabilized by the formation of a six-membered ring. Crystal x-ray diffraction techniques have been used to study this complex. The reaction time for 5-(4-nitrophenyl)-1H-tetrazole is dependent on temperature and carbon tetrachloride concentration.

4-Carboxy-2-nitrophenylboronicacid is a chemical compound with the formula (CH3CO)2NOB. It is a white crystalline solid that is soluble in water and polar organic solvents. The compound is used as a reagent for the synthesis of amino acids and peptides, and it has been shown to be an effective inhibitor of protein glycosylation by blocking the formation of alpha-dicarbonyl sugars. 4-Carboxy-2-nitrophenylboronic acid has also been used in the preparation of cyclopropane carboxylic acids.

N-Benzyl-2-nitroaniline is a quinoline derivative that has been used as an amine. It has shown to be effective in the treatment of diabetes mellitus type 2 and also possesses anti-inflammatory properties. The synthesis of this drug is based on the reaction of nitrobenzene with different amines and aluminum chloride. This reaction is followed by nitration of the resulting benzylated amides, which leads to the formation of N-benzyl-2-nitroaniline. The mechanism for this process is intramolecular hydrogen transfer from an amino group in one molecule to an electron deficient carbon atom in another molecule, forming a new bond between the two molecules. In this process, there are no reactive intermediates, such as free radicals or peroxides and it does not produce any hazardous waste products.

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3-Nitropropionic acid (3NPA) is a mitochondrial toxin that causes neuronal death by inhibiting complex enzyme activities and inducing reactive oxygen species production. 3NPA also alters mitochondrial membrane potential and induces pro-apoptotic protein expression, leading to neuronal cell death. 3NPA has been shown to be effective in the treatment of experimental models of infectious diseases, such as rat sepsis and human HIV infection, by reducing the number of activated T cells and CD4+ T cells. 3NPA also exhibits anti-inflammatory properties by inhibiting the inflammatory responses of monocytes/macrophages and neutrophils.

Please enquire for more information about 2-Chloro-3-nitrobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Fluoro-3-methyl-2-nitrobenzene is an organic solvent that has been used in the fabrication of plastics and other organic materials. It is also used as a reagent for the synthesis of pharmaceuticals, dyes, and pesticides. It may be carcinogenic to humans or animals. 1-Fluoro-3-methyl-2-nitrobenzene is metabolized by nitroreductase to form nitrosated products such as anthranilic acid, which can cause cancer. The pharmacokinetic properties of 1-fluoro-3 methyl 2 nitrobenzene have not been well studied, but it may be useful as a precursor for making new drugs.

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1,4-Bis(chloromethyl)-2-nitrobenzene is a polymerizable monomer that reacts with monomers such as vinylene and blocky to form polymers of various shapes and sizes. This compound is soluble in water. 1,4-Bis(chloromethyl)-2-nitrobenzene can be used to make polyelectrolyte materials that are stable at high pH levels. It has also been shown to be able to copolymerize with other monomers, such as vinylene and blocky. The 13C NMR spectrum shows signals for the chloromethyl group, which can be identified by the two peaks at 29.0 ppm and 33.5 ppm. Spectroscopic analysis of the polymerization products revealed a broad signal centered near 1,600 cm-1 for the sulfonium group and an absorption band near 2,000 cm-1 for the vinylene group. The polymerization

4-Nitrophenyl 2-(trimethylsilyl)ethyl carbonate is a synthetic compound that is hydrophobic and ionizable. It interacts with acid molecules and nucleic acid molecules, which are important in the process of DNA replication. 4-Nitrophenyl 2-(trimethylsilyl)ethyl carbonate can be used to synthesize an aminoglycoside by nitroaldol reaction. This chemical can also be used as a linker in transfection efficiency experiments. 4-Nitrophenyl 2-(trimethylsilyl)ethyl carbonate biodegrades quickly, making it a good candidate for drug delivery systems.

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2-Nitrophenylboronic acid is a chemical compound that is used as a substrate in the synthesis of β-amino acids. It has been shown to inhibit replication and cyclic nucleotide phosphodiesterase activity. 2-Nitrophenylboronic acid also has anti-inflammatory effects and can be used to treat inflammatory diseases. Its light emission characteristics make it an ideal candidate for use in optical imaging techniques, such as fluorescence microscopy. The hydroxy group on the 2-nitrophenylboronic acid molecule enables the compound to react with other molecules to form a variety of covalent bonds, which is important for its biological function.

2-Chloro-5-nitrotoluene (2CNT) is an organic compound that is used as an intermediate in the synthesis of dyes and pharmaceuticals. It is a potent carcinogen, mutagen, and hepatotoxin. 2CNT can be synthesized from nitrobenzene and hydrochloric acid by a three-step process: nitration to form the corresponding nitro compound, followed by chlorination with chlorine gas to form 2CNT. The industrial preparation of 2CNT includes the following reaction yield: The molecular modeling of 2CNT shows it has a dihedral angle of 180° with one unshared electron pair on each carbon atom. This type of geometry allows for the molecule to rotate freely, which results in its relatively high transport properties.

5-Nitroisophthalic acid monomethyl ester (NIAE) is an acetylating agent that can be used for the preparation of 5-nitroisophthalic acid, which is a precursor to the synthesis of dyes and pharmaceuticals. The acetylation reaction of NIAE with proteins produces an insensitive material. Acetylation also inhibits the activity of serine proteases and virus replication. In addition, it has been found that the catalytic reduction of NIAE with palladium is faster than other synthetic methods. Optimal reaction conditions are obtained by adding chloride ions to the reaction mixture, while reductive conditions are optimal for catalysis. Reaction time can be shortened by using a soluble catalyst such as iodide ion or mercury(II) sulfate. The active site of NIAE contains a nitro group that reacts with substrates in the presence of oxygen, forming a product from which the acetyl group has been removed

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L-Methionine 4-nitroanilide is a polymerase chain reaction (PCR) substrate. It has been shown to bind to DNA with calcium and to have protease activity. L-Methionine 4-nitroanilide is a synthetic substrate used in the biochemical study of serine proteases. L-Methionine 4-nitroanilide has been found to be active against P. aeruginosa and thermococcus, but not against mosquitoes. The optimum pH for this compound is 7 and it can be found at a concentration of 10mM in the range of pH 5 - 8.

Please enquire for more information about 1-(2-Cyano-4-nitrophenyl)piperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

(R)-(-)-N-(3,5-Dinitrobenzoyl)-a-phenylglycine ((R)-DBBG) is a chiral molecule that is used as an anthelmintic drug. It is a derivative of the amino acid glycine and has been shown to inhibit angiogenesis in cancerous tumors. (R)-DBBG inhibits fatty acid synthesis by binding to the acyl carrier protein and inhibiting the conversion of acetate to malonyl coenzyme A. This inhibition leads to a depletion of long-chain fatty acids, which can be detected by chromatography. The enantiomers have been shown to have different effects on rat liver microsomes, with one enantiomer being more potent than the other. The kinetic studies show that the amines react with R-DBBG and form an intermediate with a reactive α1-acid glycoprotein, which subsequently reacts with hydrogen peroxide and forms a reactive intermediate that decom

2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide is a chemical compound that has been studied using molecular modeling. It is an example of a control agent that can be used to inhibit the polymerization of styrene monomers and thereby reduce the concentration of styrene, which is a known carcinogen. 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide has been shown to have an activation energy of 28.6 kJ/mol and can be synthesized by reacting styrene with nitroethane. This molecule also contains a fluorescent chromophore that has been shown to be sensitive to changes in the polymer concentration, making it possible to measure the amount of styrene present in a system.

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Ethyl 3-hydroxy-2-nitrobenzoate is a versatile building block in organic synthesis. It is a useful intermediate that can be used for the synthesis of complex compounds, research chemicals and reagents. It is also a useful scaffold for the synthesis of fine chemicals, and has been used as a reaction component in high quality chemical reactions.

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4-Bromo-2-nitrocinnamic acid is a naturally occurring amino acid that is a component of wheat, carrots, and cereals. It is an enzyme inhibitor and has been found to be stable under heat treatment. 4-Bromo-2-nitrocinnamic acid has been shown to inhibit the activity of 3 lysine hydrolase enzymes (LysE1, LysE2, LysE3) in vitro. This inhibition decreases lysine levels and may have health implications for infants fed with 4-bromo-2-nitrocinnamic acid treated wheat flour. The efficiency of 4-bromo-2 nitrocinnamic acid as an enzymatic inhibitor for these enzymes was determined by measuring the release of free lysine from various substrates at different concentrations of the inhibitor. These parameters were then used to calculate the theoretical inhibition percentage for each substrate at a given concentration.

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O-(4-Nitrophenyl)hydroxylamine (OPH) is an enantioselective, catalytic, and thermal stable reagent for the synthesis of chiral methyl groups. OPH can be used as a nucleophile to convert electron-deficient alkenes into α-chloroalkenes. It also reacts with nitroarenes to give nitroalkenes in high yields. OPH has been shown to be effective in the asymmetric hydrolysis of esters and amides through its ability to oxidize the methyl group on the substrate. This reaction does not occur with other groups such as hydroxyl or hydrogen atoms. Methyl groups are important for many biological molecules, including proteins and nucleic acids, which form the backbone of cells that make up living organisms. The OPH reaction is catalyzed by enzymes called methyltransferases, which transfer one atom of methyl from S-adenosylmethionine (SAM)

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3-Nitro-4-hydroxyquinoline is a quinoline derivative that shows anticancer activity. It has been shown to inhibit the growth of human epidermal cells by inhibiting the proliferation of epidermal growth factor receptor (EGFR) and its downstream signaling pathways. 3-Nitro-4-hydroxyquinoline also inhibits HIV infection by binding to the viral envelope protein gp120, which prevents it from binding to or entering host cells. 3-Nitro-4-hydroxyquinoline is classified in cycle analysis as an industrial chemical. Its molecular modeling suggests that this drug binds to the mitochondrial membrane potential, enhancing 4-hydroxyquinoline's effects on cancer cell death.

(4-Nitrophenyl)phenylamine is an ionization technique used to measure the concentration of copper oxide in a sample. It is classified as a chemical ionization technique, which uses electron impact or chemical reactions to produce ions. The reactant gas is usually hydrogen chloride, and the reaction vessel is heated to produce an atomized spray of copper oxide particles that are then ionized. The copper oxide particles are collected on a solid phase microextraction fiber and then analyzed by measuring the amount of current between two electrodes.

4-(2-Hydroxyethylamino)-3-nitrophenol is a nitrophenol that can cause toxicity in humans. It has been investigated for its potential use as a treatment for erectile dysfunction. The compound was found to have a long half-life of over 24 hours, which may be due to its slow metabolism by esterases and glucuronidases. 4-(2-Hydroxyethylamino)-3-nitrophenol has been shown to be an allergen and is toxic to the skin, lungs, and muscles. This chemical can cause cancer when it is irradiated or mixed with other chemicals such as 4-amino-2-nitrophenol (ANP).

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2-Chloroacetyl-5-nitrobenzophenone (2-CNBP) is a benzohydrazide derivative that is used as an intermediate in the synthesis of 2-chloroacetyl-5-nitrobenzophenone methanesulfonate (CANB), which is a potent herbicide. The crystal structure of 2-CNBP has been determined by X-ray diffraction and found to be monoclinic. 2-CNBP has been shown to inhibit angstrom, which are enzymes that transfer acetyl groups from acetyl coenzyme A to pyruvate during carbohydrate metabolism. It also inhibits methanol dehydrogenase, an enzyme that converts methanol to formaldehyde and then formate.

5-Fluoro-2-nitroanisole is an aminophenol that has potent inhibitory activity against lung cancer cells. This agent inhibits the growth of cancer cells by methylating the epidermal growth factor receptor (EGFR) and preventing its activation. 5-Fluoro-2-nitroanisole also inhibits the production of epidermal growth factor, which is a potent mitogen for skin cells. In vitro cytotoxic activity was observed when this compound was combined with heat or ultraviolet light.

4-(N-Methyl-N-nitrosamino)-4-(3-pyridyl)butanal is a nitrosamine that has been found to be carcinogenic in long-term studies. It has been shown to induce tumorigenesis in vitro, and it has been detected in the saliva of smokers. 4-(N-Methyl-N-nitrosamino)-4-(3-pyridyl)butanal has also been shown to have genotoxic potential by highlighting oxidative DNA damage and mutagenicity. This compound is an aldehyde that can react with aminopyrine to form an N,O-acetal adduct, which can then bind covalently with DNA. The genotoxicity of this compound may be due to its ability to form reactive oxygen species by reacting with nitrous oxide (NO).

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Applications Intermediate in the preparation of nitro substituted quinazolones. References Sirisoma, N., et al.: J. Med. Chem., 52, 2341 (2009), Zeng, X., et al.: Bioorg. Med. Chem. Lett., 20, 6282 (2010),

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5-Bromo-3-nitro-2(1H)-pyridinone (5BNP) is a synthetic posttreatment reagent that is soluble in water and hydrochloric acid. 5BNP has been shown to be an effective catalyst for the synthesis of tetracyclic synthons, which are chemical building blocks used in organic chemistry. The use of 5BNP as a catalyst offers some advantages over other methods, such as being more economical and environmentally friendly. The reaction process is also streamlined and simple to carry out, making it an ideal starting point for introducing new chemists to this area of research.

5-Chloro-2-nitroanisole is a solvent that has been shown to have vibrational properties. It has been used in the determination of formamide, which is an organic compound with a pungent odor. This chemical can be used as a probe for membrane potential, and it has been used in mitochondrial membrane potential studies. 5-Chloro-2-nitroanisole is reactive and nucleophilic and has high solubility in water. The sample preparation for 5-chloro-2-nitroanisole includes chromatographic methods, such as gas chromatography or liquid chromatography. Chromatographic science is the study of how to separate mixtures of chemicals on a solid or liquid support by passing them through a stationary phase that interacts differently with each component. 5-Chloro-2-nitroanisole also has antiproliferative effects on hCT116 cells, which are cancer cells derived from human

3-Fluoro-4-nitrobenzonitrile is a diamine that is activated by a nitro group and a halogen. It can be used as an intermediate in the synthesis of other chemicals, such as dyes, pharmaceuticals, and pesticides. 3-Fluoro-4-nitrobenzonitrile is also used to synthesize nitroaminobenzenes, which are converted to aminonitriles by reaction with ammonia. Nitro groups on 3-fluoro-4-nitrobenzonitrile react with alcohols to form nitrosamines. 3-Fluoro-4-nitrobenzonitrile has been shown to be effective in the treatment of angina pectoris and myocardial infarction due to its ability to dilate coronary arteries.

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