Nitro

Please enquire for more information about Ethyl 6-nitro-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Amino-5-nitro-2,1-benzisothiazole is a diazonium salt that is used in wastewater treatment. It reacts with hydrogen peroxide to produce an unstable amine and a stable glycol ether. This process is known as the 3ABA reaction. The amine can be cleaved by water to produce ammonia and nitrous acid. Nitrous acid can react with organic matter in wastewater to form nitrate salts, which are soluble and easily removed from the wastewater stream. 3-Amino-5-nitro-2,1-benzisothiazole is also used in the manufacture of polyethylene terephthalate (PET) plastics. PET plastics are resistant to staining and have excellent color clarity.

2-((2-(2-Hydroxyethoxy)-4-nitrophenyl)amino)ethanol is a fatty acid that is used as a conditioning agent in hair and skin care products. It is also an ingredient in toothpastes, mouthwashes, and chewing gum. 2-((2-(2-Hydroxyethoxy)-4-nitrophenyl)amino)ethanol is classified as a cationic surfactant and has been shown to have a low toxicity profile. It can be hydrated or anhydrous with the chloride form being more stable. The molecular weight of 2-((2-(2-Hydroxyethoxy)-4-nitrophenyl)amino)ethanol ranges from 178.24 g/mol for the anhydrous form to 202.33 g/mol for the hydrated form. This product may also be known by its chemical name: sodium 2-(2-(2-hydroxyethoxy)-

Please enquire for more information about 4-Chloro-2-nitro-1-(phenylmethylthio)benzene including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromo-6-nitrophenol is a synthetic chemical that is used as an intermediate in the synthesis of other chemicals. It can be prepared by reacting ammonium formate with hydroxyl group of 2-bromo-6-nitropyridine. The reaction yield can be improved by activating the hydroxyl group and removing impurities through a dehydration reaction. The time required for the reaction to occur can be shortened by using acetonitrile as a solvent instead of water. This chemical is also synthesized by coupling metal salts with nitro groups or amines, which are called Suzuki coupling reactions.

6-Nitrobenzo[d]oxazole is a nitroarene that can stabilize DNA by forming covalent bonds to the N7 position of guanine. It has been shown that this compound is able to inhibit topoisomerase I, an enzyme involved in DNA replication, and topoisomerase II, an enzyme involved in DNA recombination. 6-Nitrobenzo[d]oxazole has been shown to be active against cancer cells and inhibits cancer cell proliferation. This compound also interacts with hydrogen bond acceptors on the surface of cancer cells and has been shown to inhibit the growth of these cells as well as their ability to invade other tissues.

N,N-Bis(4,4,4-Trifluorobutyl)Nitrous Amide is a nitrosamine that is metabolized by cytochrome P450 to form 3-methylamino-1,2,4-trinitrobenzene. The carcinogenic potential of this compound has been evaluated in Sprague Dawley rats. The carcinogenicity of N,N-bis(4,4,4-Trifluorobutyl)Nitrous Amide was observed to be multifocal with malignant changes in the bladder and liver in both sexes. This compound also has pharmacokinetic properties that are characterized by a high affinity for proteins and a low clearance rate. !--END-->

4-Hydroxy-4'-nitrobiphenyl is a bifunctional molecule that can be used to reduce nitrate pollution. This compound has a high catalytic activity for hydroxylase, which is an enzyme that catalyzes the conversion of 4-hydroxy-4'-nitrobiphenyl to 4-hydroxybiphenyl. The compound also has the ability to photocatalyze biphenyl and aspergillus parasiticus. It can be used to treat environmental pollution with nitrate and other pollutants. Sensors have been developed using this compound that are sensitive enough to detect as little as 1 nanomolar of pollutant in water.

2-(4-Nitrophenyl)thiazole is a chemical compound that can be used as an oxidase inhibitor. This product is an organic solvent with a boiling point of about 190 °C at atmospheric pressure. It has been shown to inhibit the activity of xanthine oxidase and xanthine dehydrogenase, with IC50 values of 0.25 mM and 6.1 mM, respectively. 2-(4-Nitrophenyl)thiazole has also been shown to inhibit the oxidation of xanthine by alkaline xanthine oxidase in aprotic solvents.

4-Nitroisoquinoline is a nitro compound that can be synthesized from 4-nitrotoluene. It is a nucleophilic reactant and has been used in biomolecular synthesis. 4-Nitroisoquinoline is also hydrated and has two isomers, the α and β forms. The α form can be produced by reacting with sodium hydroxide, while the β form can be produced by reacting with sodium methoxide. This chemical has been shown to have phosphatase activity as well as covalent and ionic forms. Hydration of 4-nitroisoquinoline produces 2 molecules of water per molecule of chemical, which may account for its high yield.

N,N-Dimethyl-4-nitroaniline is a chemical compound that belongs to the group of nitro compounds. It is an intermediate in the synthesis of other chemicals such as N,N-dimethylaniline, 4-nitrodiphenylamine, and 2-nitrophenylhydrazones. The vibrational and photochemical properties of this molecule are similar to those of nitromethane. N,N-Dimethyl-4-nitroaniline has a molecular weight of 166.24 g/mol and its solubility in water is less than 1 g/100 mL at 25°C. This substance has been shown to be stable under hydrochloric acid conditions with no evidence for hydrogen bonding or dipole formation between molecules. This chemical compound also shows low fluorescence intensity in nonpolar solvents.

2-Chloro-4-methyl-6-nitroquinoline is a promyelocytic leukemia (PML) treatment drug that is used to inhibit the growth of leukemia cells. It has been shown to be effective in inducing the death of leukemia cells in vitro and in vivo. This activity is due to its ability to bind and inhibit topoisomerase II, which prevents the unwinding of DNA strands during replication. 2-Chloro-4-methyl-6-nitroquinoline also inhibits multidrug resistance, which may be due to its ability to induce cytotoxicity. The following product descriptions are generated from the information given above: Rifapentine is an anti-tuberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. Rifapentine inhibits bacterial growth by binding to DNA dependent RNA polymerase

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

2-Methyl-3-nitrophenylacetic acid is an alkali metal, which is obtained by the condensation of 2-methylphenol and nitric acid. The synthesis of this compound can be achieved through catalytic reduction of the nitro group with hydrogen in the presence of a nickel catalyst. This method has been shown to produce high yields. 2-Methyl-3-nitrophenylacetic acid is mildly toxic to humans and animals. It is a dopaminergic agent that has been used as a precursor for the production of ropinirole hydrochloride, which is used in the treatment of Parkinson's disease.

Please enquire for more information about N-(2-chloro-5-nitrophenyl)-3-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-[(4-Nitro-1H-pyrazol-1-yl)methoxy]benzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page