Nitro

Stability Hygroscopic Applications N-(3-Hydroxypropyl) 4-hydroxy-2-nitroaniline is a hair ingredient. It is used as a semipermanent (nonoxidative) hair colorant and as a toner in permanent (oxidative) hair dye products. 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 Burnett, C. L., et al.: Int. J. Toxicol., 28, 217S (2009); Yazar, K., et al.: Contact Dermatitis, 61, 269 (2009)

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7-Nitrobenzo[d]thiazol-2-amine (NBDTA) is a nitrogenous coordination compound that contains both endocyclic and exocyclic nitrogens. It is a hexacoordinated molecule with two nitrogens in the endocyclic position and three nitrogens in the exocyclic positions. The infrared spectrum of NBDTA has been recorded at 707 cm-1, which corresponds to an N-H stretching vibration. This compound can form adducts with thiols, silicon, and ammonia as well as 2-aminothiazole and 2-amino-5-methylthiazole.

1-Methyl-4-nitro-1H-imidazole-5-carboxamide is an amide that has a mass of 99.9997 and is the most stable of its isomers. 1MNCA is used as a reagent in ion cyclotron resonance experiments, as well as in electron transfer and elimination experiments. The proton transfer process from 1MNCA to H3O+ was observed using proton probes. It also reacts with nitrous acid to form the anion and cation, which can be detected by electron or mass spectrometry. This compound has been shown to react with singlet oxygen and hydrogen peroxide, yielding the corresponding nitroxides and hydroxyl radicals respectively.

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2-Bromo-6-nitrobenzaldehyde is a chemical compound that can be synthesized by the reaction of hydrogen chloride and 2-bromoacetophenone. Mechanistically, this reaction proceeds through chlorination of the indole ring, which causes protonation and ring closure. The resulting product undergoes hydrochloric acid catalysis to form a dithioacetal, which is then chlorinated with chloroform to produce the final product. The bromine atom in 2-bromo-6-nitrobenzaldehyde is substituted with chlorine to create 2-chloro-6-nitrobenzaldehyde. This substitution changes the reactivity of the molecule, as well as its physical properties.

5-Methyl-2-nitrophenylacetic acid (5-MPA) is a metabolite of the drug pentoxifylline. It is used as a screening tool for platelet aggregation and as a diagnostic agent for ketoacidosis. 5-MPA has been shown to be metabolized by arachidonic acid synthase in vitro, but does not appear to inhibit arachidonic acid synthesis or metabolism in vivo. It has been shown to have hypoxic effects, which may be due to its ability to inhibit the synthesis of cyanide by inhibiting cytochrome oxidase.

Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is a fluorescent marker that can be used in immunohistochemical staining. It binds to endogenous vasoactive intestinal peptide, calcitonin and other proteins in tissues and can be detected using immunostaining. Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is optimised for use as a substrate for neutral endopeptidase and metalloendopeptidase enzymes, which are responsible for the degradation of vasoactive intestinal peptide.

2,6-Dinitrotoluene is an intermediate in the synthesis of explosives. It is a metabolite of 1,2,4-trinitrotoluene (TNT) and has been shown to be genotoxic in CD-1 mice. 2,6-Dinitrotoluene has been found to have toxicological effects on tissue culture cells (e.g., inhibition of DNA and protein synthesis). The metabolic fate of 2,6-dinitrotoluene is not well understood and may involve glucuronide conjugation or intramolecular hydrogen transfer. In vitro studies have demonstrated that 2,6-dinitrotoluene can act as a solid catalyst for fatty acid oxidation reactions.

4-Nitro-1H-pyrazole-3,5-dicarboxylic acid is a coordination compound that belongs to the class of dioxane. It has been shown to catalyze the hydrolysis of carboxylic acids and the oxidation of aminoguanidine. The crystallographic study of the sodium salt of 4-nitro-1H-pyrazole-3,5-dicarboxylic acid revealed a molecule with a square pyramidal geometry. The nitro groups are positioned in such a way that they can easily be impacted by an electron, which may lead to an increase in reactivity. This compound also forms stable complexes with oxygen atoms and can act as an anion.

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3-Nitro-4-chlorobenzaldehyde is a copper complex that has been used in the study of molecular interactions. The molecule has been studied by a number of techniques, including binding experiments, vibrational spectroscopy, and light emission. 3-Nitro-4-chlorobenzaldehyde has shown bacteriostatic activity against Escherichia coli and Bacillus subtilis. This compound also appears to have potential as a drug target due to its ability to inhibit the growth of Pseudomonas aeruginosa. 3-Nitro-4-chlorobenzaldehyde may be useful in the treatment of industrial processes involving nitric acid.

2-Cyano-3-nitropyridine is an aniline that inhibits protein kinases. It has been shown to inhibit the activity of protein kinases in vitro and in cellular assays. This agent also has potent anti-inflammatory properties, inhibiting prostaglandin synthesis by blocking the enzyme cyclooxygenase. 2-Cyano-3-nitropyridine is able to inhibit inflammation in vivo with a potency comparable to that of indomethacin. The mechanism of action for this drug is unknown, but may be due to its ability to inhibit the production of reactive oxygen species or nitric oxide.

7-Chloro-1,2,3,4-tetrahydro-1-(2-methyl-4-nitrobenzoyl)-5H-1-benzazepin-5-one is a synthetic intermediate that is used in the synthesis of tolvaptan. It is a white solid that can be synthesized from 7-chloroquinoline and 2-(methylsulfonyl)benzoic acid by acylation with oxalyl chloride. The crude product can be purified by recrystallization or column chromatography. 7C7TBT has a molecular weight of 313.85 g/mol and an empirical formula of C14H11ClN2O3S. It is soluble in chloroform and ethanol but insoluble in water.

4-Fluoro-3-nitrophenylacetonitrile is a monomer that can be synthesised from the reaction of carbamic acid and diphenyl ether. It is chiral, stereoselective and nucleophilic. 4-Fluoro-3-nitrophenylacetonitrile can also be synthesised by reacting fluoroacetamide with sodium cyanide in water, forming the corresponding amide, which reacts with acetonitrile to form the nitro compound. The anti-cancer properties of 4-fluoro-3 nitrophenylacetonitrile have been studied in vitro and in vivo. This substance has been shown to inhibit growth of cancer cells and induce apoptosis. In addition, this substance has been used as a synthetic strategy for dihydroisoquinolines, which are important for their anti-cancer properties.

2,3,5,6-Tetrafluoronitrobenzene is a phenoxy compound that is synthesized by the reaction of 2,3,5,6-tetrafluoroaniline with dimethylformamide and halides. The functional groups present in this compound are fluorine, nitro and phenoxy. This compound has been studied for its use as an acceptor in styrene polymerization catalyzed by palladium. It also can be used to produce molecular ions after reacting with styrene and a base such as sodium methoxide. The product of this reaction is the nitrophenolate ion. This type of ion can be used as a constant in organic reactions.

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2'-Hydroxy-5'-nitrohexadecanamide sodium is a reagent that can be used for a variety of laboratory reactions. It is a versatile building block, useful intermediate, and useful building block for complex compounds. This compound has also been shown to be useful in the synthesis of pharmaceuticals and other fine chemicals.

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1-Isocyanato-4-methoxy-2-nitrobenzene is an efficient and convenient method for the synthesis of N,N'-disubstituted amides. This reaction can be carried out with a variety of functional groups present in the amide, including sterically hindered amides. The methodology can be applied to a wide range of aromatic amines and is applicable to many synthetic methods.

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3-(4-Nitrophenyl)pentanedioic acid is a synthetic intermediate that can be used in the synthesis of various organic compounds. This compound has been used as an intermediate for the synthesis of pharmaceuticals, pesticides, and dyes. The synthesis of 3-(4-Nitrophenyl)pentanedioic acid proceeds through a multicomponent reaction involving both high-yielding steps and low-yielding steps. The yields are typically around 70% for each step.

The synthesis of the Z-L-alanine 4-nitrophenyl ester is an incubated and synthetic process. It is a stable complex with methyl esters, formed by interaction with esterases. The stoichiometry of this reaction is 1:1. The Z-L-alanine 4-nitrophenyl ester hydrolyzes to L-alanine and 4 nitrophenol. This product has been shown to be stable in horse, leucocyte, and pancreatic homogenates.

3,6-Dinitro-1,8-naphthalenedicarboxylic anhydride is a fine chemical that is used as a building block in the synthesis of other compounds. It is also used as a reagent and can be found in research chemicals with CAS No. 3807-80-5. 3,6-Dinitro-1,8-naphthalenedicarboxylic anhydride is versatile and has many uses as a reaction component. The compound can be used to produce complex compounds or scaffolds that are useful in research.

Isonitrosoacetone is a compound that has been synthesized from methyl ethyl pyridinium chloride and hydrogen chloride. This compound is a coordination geometry molecule with a pyridine ring in the center, which contains two nitro groups. Isonitrosoacetone has been shown to be effective in cleaning detergent compositions, as well as being an animal-safe chemical. Isonitrosoacetone also reacts with β-unsaturated ketones to form stilbene derivatives.

CAS No. 137391-68-5 is a fine chemical that is used as a building block in organic chemistry research and as a reagent, speciality chemical, or intermediate. This compound has been shown to be useful in the synthesis of complex compounds and can be employed as a versatile building block for the synthesis of pharmaceuticals and other chemicals. This compound has also been shown to be an excellent reaction component, making it an ideal scaffold for the construction of larger molecules.

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4,5-Dichloro-2-nitroaniline is a chemical compound that has been shown to be an uncoupler of oxidative phosphorylation in ciliates. It is experimentally shown that the reaction yield for 4,5-Dichloro-2-nitroaniline is much higher than that of the corresponding methylbenzene. The two isomers are not detected in the gaseous phase, but only as products of thermal decomposition at high temperatures. Linear regression analysis and predictive models were used to evaluate the transfer and population growth rates at different temperatures. Narcosis was observed in rats exposed to 4,5-Dichloro-2-nitroaniline at concentrations greater than 0.1 ppm (0.1 mg/L).

4-Nitrobenzyl bromide is a reactive compound that reacts with the hydroxyl group of phenols to form 4-nitrophenols. It has been shown to react with congestive heart failure (CHF) patients' sera and bind to receptors on the surface of red blood cells, thereby inhibiting their ability to carry oxygen. The reaction mechanism for this process is unclear, but it is thought that it may involve a nucleophilic attack on the double bond in the phenol by a hydroxyl radical. This chemical can also be used as an analytical method for determining organic acids in natural compounds. Monoclonal antibodies are used for this purpose because they are specific for certain organic acids and thus will only react with them.

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Pentachloronitrobenzene is a chemical that belongs to the group of nitrobenzenes. It is used as a biochemical reagent in enzyme assays, including methyl transferase, matrix effect, and chinese herb. Pentachloronitrobenzene can be used to detect single nucleotide polymorphisms (SNPs) in genes. The compound is also used as an analytical method for measuring acute toxicities and enzyme activities. In addition, pentachloronitrobenzene has been shown to have antibacterial properties against a wild-type strain of Escherichia coli with fluorescence probe.

2-Nitroterephthalic acid is an inorganic acid that belongs to the nitro group. It is a white powder and has a melting point of 115°C. The crystal structure of 2-nitroterephthalic acid was determined using x-ray crystallography, and the thermal expansion coefficient was measured at different temperatures between 10° and 120°C. This compound has been used as a test sample to study the hydrogen bonding interactions between methyl ethyl groups on the molecule's surface with carboxylate groups in other molecules. Structural analysis of this compound also revealed that it contains a carboxylate group that can be converted into an ester for use in organic synthesis.

2-Bromo-3-methoxy-6-nitropyridine is a nicotinic antagonist that prevents acetylcholine from binding to nicotinic acetylcholine receptors. It has been shown to be effective in the treatment of pain in humans. This drug is a synthetic compound that has been shown to inhibit epibatidine induced emission and hydrogenolysis, as well as block the binding of epibatidine to nicotinic acetylcholine receptors. The affinity of 2-bromo-3-methoxy-6-nitropyridine for neuronal nicotinic acetylcholine receptors is approximately 10 times less than that of nicotine.

3-Bromo-4-nitrobenzaldehyde is a natural product that has been synthesized. It is used in the synthesis of vancomycin, an antibiotic that can inhibit bacterial growth by binding to the peptidoglycan layer and inhibiting the synthesis of bacterial cell walls. 3-Bromo-4-nitrobenzaldehyde contains a nitro group, which is an ether. The nitro group reacts with aryl halides to form a nitroaryl ether, which undergoes nucleophilic substitution. 3-Bromo-4-nitrobenzaldehyde also reacts with sodium bicarbonate to form sodium bromide and carbon dioxide gas.

2,4-Dinitrophenetole is a nucleophilic compound that reacts with the hydrogen bond of an acid. It is a thermodynamic and kinetic acid which reacts with bile acids in the second order. The rate enhancement of 2,4-dinitrophenetole is due to its uncoupling effect on hepg2 cells. This chemical has been shown to react faster with picric acid than with nitric acid solutions.

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5-Amino-6-[(N-methyl-N-nitroso)amino]-7-methylquinoline (5AMQ) is an endophytic isolate from the plant Nigrum, which has shown to be a potent antimicrobial agent. 5AMQ inhibits the growth of bacteria by inhibiting the synthesis of proteins and nucleic acids. It also inhibits phosphate uptake in bacteria, leading to depletion of energy stores. This compound has been shown to have a beneficial effect on fertility in mammals when administered orally. 5AMQ has been used as a bioassay for the discovery of other bioactive compounds from Nigrum and other plants.

Intermediate in the synthesis of afatinib

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N-Nitroso akardite II is a nitrosating agent that can be used as a versatile building block for the synthesis of complex compounds. It is also a useful scaffold and intermediate, and has been shown to be an effective reagent in organic syntheses. N-Nitroso akardite II is an excellent high quality research chemical with a CAS No. 1076199-26-2.

2-Acetamido-5-nitrobenzoic acid methyl ester is an organic molecule that has the chemical formula C7H6N2O4. This compound belongs to a class of compounds called diazo compounds, which are characterized by a nitrogen atom with two bonds to carbon atoms and one bond to oxygen. 2-Acetamido-5-nitrobenzoic acid methyl ester is soluble in water and methanol. It has been shown to be chiral and exhibits optical activity. The experimental results show that the compound can exist in two different forms or conformations, which are distinguished by their x-ray diffraction patterns. These conformers have been identified as (1) the protonated form and (2) the torsion form. The protonated conformer has a molecular structure that contains a benzene ring with a hydrogen atom attached to it, while the torsion conformer does not contain this hydrogen atom

2-Fluoro-6-nitrobenzenesulfonyl chloride is a synthetic compound that has been shown to be effective in the treatment of cancer. It inhibits translation by binding to the ribosome and blocking the activity of the ribosomal RNA molecule. 2-Fluoro-6-nitrobenzenesulfonyl chloride also has an effect on DNA synthesis, which may be due to its ability to inhibit noninvasive positron uptake. This agent has been shown to be nontoxic in vitro and is stable when used with cells.

Applications 2,4-Dinitrobenzenesulfonic Acid (cas# 89-02-1) is a useful research chemical.

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2,4-Dichloro-5-nitrophenol is a synthetic chemical that is used in the production of sodium carbonate. The chemical can be synthesized by the reaction of phosphorus oxychloride with nitrophenol and sodium carbonate. 2,4-Dichloro-5-nitrophenol has been shown to be an effective inhibitor of phosphorus removal from wastewater and has been studied as a potential replacement for chlorine compounds in industrial processes.

4-Hydroxy-3-nitrobenzonitrile is a lipid molecule that is structurally similar to aniline. It has been shown to be an inorganic analyte and desorption/ionization mass spectrometry matrix. It can be analyzed using laser desorption/ionization mass spectrometry, which enables the identification of proteins and other molecules. 4-Hydroxy-3-nitrobenzonitrile can also be analyzed using UV absorption, which is useful for determining the purity of samples.