Nitro

Please enquire for more information about 4-Amino-2-nitrodiphenylamine-2'-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Methyl 3-[(4-nitrobenzyl)oxy]benzoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-{[2-Nitro-4-(trifluoromethyl)phenyl]thio}-1-phenyl-1H-tetrazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5- Nitro- 1H- [1, 2, 4] triazole- 3- carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Amino-4-methyl-5-nitrobenzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(4-Nitrophenoxy)aniline is a synthetic drug that is used as a substrate for the cytochrome P450 system. It has been shown to be metabolized by the liver in two steps, forming reduction products and interacting with thiourea. This drug also has functional groups which are active in the group p2 of the periodic table, such as diphenyl ethers and aminophenols. 4-(4-Nitrophenoxy)aniline can be used to probe the interaction between an enzyme and its substrate.

Please enquire for more information about 2-(4-Methyl-1H-pyrazol-1-yl)-5-nitrobenzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Nitro-2-(phenylthio)benzoic acid is an efficient and versatile synthetic intermediate for a wide range of organic compounds. It has been synthesized from n-phenylanthranilic acid, potassium carbonate, and potassium nitrate. The synthesis can also be carried out using carbonates such as sodium or calcium, which are more readily available. 5-Nitro-2-(phenylthio)benzoic acid is prepared by the amination of an alkylamine with nitric acid followed by heating to superheat the reaction mixture. This process yields the desired product in high yields (90%). The compound is also used to produce other derivatives such as phenylnitrosamine and 2,3-dinitrophenol.

3-Nitro-benzene-1,2-diol is an inhibitor of catechol-o-methyltransferase (COMT), which catalyzes the transfer of a methyl group from S-adenosyl methionine to dopamine. This results in the formation of 3-O-(methylamino) catechol. COMT inhibitors are used as pharmaceutical preparations for the treatment of Parkinson's disease and other diseases involving dopamine. 3-Nitro-benzene-1,2-diol has been shown to inhibit COMT and prevent the breakdown of dopamine in the brain, which may be beneficial for treating Parkinson's disease and other nervous system diseases.

Please enquire for more information about 2-Fluoro-6-O-[2-(4-nitrophenyl)ethyl]-2’-dexoyinosine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Nitrophenyl chloroacetate (4NPCA) is a chemical compound that is used in the synthesis of cis-UCA, an inhibitor of ornithine decarboxylase. 4NPCA is synthesized by adding a solution of 4-nitrophenol and acetyl chloride to a suspension of urea. The reaction proceeds through an intramolecular hydrogen transfer from the nitro group to urea, forming cis-UCA and 4NPCA. The process is accelerated by thermodynamic, kinetic, and carbonic effects. Reaction rates are dependent on the pH of the solution. Protons stabilize the intermediate species that form during the reaction mechanism. The stabilizing effect of protons slows down the rate at which intermediate products are formed. Gels containing erythrocyte proteins can be used to separate cis-UCA from 4NPCA using gel chromatography.

1-(4-Nitrophenyl)-1H-pyrrole-2-carbaldehyde (1NPCA) is a nitrogenous compound that has been shown to react with alkaline solutions. The reaction between 1NPCA and an alkaline solution can occur in the presence or absence of a solvent. This reaction yields p-nitrophenol, which can then be oxidized to yield nitrobenzene. The addition of chloroform to this mixture leads to the formation of chloronitrobenzene. In acidic conditions, 1NPCA reacts with succinimide to form 1-(4-nitrosulfonyl)pyrrole, which can be further oxidized by permanganate to yield 4-nitrosodimethylamine.

Please enquire for more information about N-(2,4-Dimethyl-6-nitrophenyl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

Please enquire for more information about 2-Methyl-5-nitronicotinicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(4-Methyl-3-nitrophenyl)acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Hydroxy-3-nitrocoumarin (4HNC) is a synthetic compound that is used as an antimicrobial agent. It is synthesized by reacting sodium carbonate with the reaction products of copper complex with coumarin derivatives. 4HNC has an intramolecular hydrogen bond and a frequency shift, which can be seen on spectroscopy. The crystal structure of 4HNC has been determined using x-ray crystallography. This active form inhibits bacterial growth by interacting with the carboxylate group in the enzyme nitro reductase and hydroxyl group in soybean lipoxygenase. It also inhibits biological properties such as nitric oxide production and lipid peroxidation, which are important factors in inflammation. 4HNC shows potent inhibitory activity against nitro, soybean lipoxygenase, and other enzymes involved in inflammatory processes.