Nitro

3-Nitrobenzaldehyde is an organic compound that is used in the synthesis of monoclonal antibodies for use in cancer research. It has been shown to have genotoxic and carcinogenic effects, as it binds to nucleic acids and inhibits DNA replication. 3-Nitrobenzaldehyde has been shown to be effective against a variety of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. This compound also inhibits protein synthesis by binding with amines and hydrogen bonding with the amino acid residues of proteins.

4-Nitrophthalic acid is a white crystalline solid that has an acid and basic character. It has been shown to be antigenic, with a specific antibody able to bind to the 4-nitro group. The structure of 4-Nitrophthalic acid was determined using X-ray crystallography and NMR spectroscopy. The molecular weight of 4-Nitrophthalic acid is 177.2 g/mol, with a melting point of 174 °C and a boiling point of 341 °C. It is soluble in water and organic solvents such as ethanol, acetone, chloroform, ethyl ether, benzene, hexane, dichloromethane and ethyl acetate.

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.

4-Methoxy-3-nitroaniline is a chemical compound that has been shown to have anti-tumor and anti-inflammatory effects. It belongs to the class of amines and can be synthesized by nitrating 4-methoxy aniline. The reaction product is then reacted with sodium hydroxide in a solution of alcohol and water, which produces 2,4-dinitroaniline. When this substance is heated at high temperatures, it converts into a mixture of products, including 2,4,6-trinitroaniline. This compound has been shown to inhibit tumor growth in rats. Toxicity studies revealed that it was not toxic when administered orally in doses up to 5g/kg body weight for 7 days.

3-Hydroxy-4-nitrobenzoic acid is a hydroxybenzoic acid that has been used for the synthesis of other compounds. It is an intermediate in the Friedel-Crafts reaction, which involves the conversion of 3-hydroxybenzoic acid to 3-ethylbenzthiazoline-6-sulfonic acid. It also forms reaction products with p-hydroxybenzoic acid and 5-nitrosalicylic acid as well as monosodium salt. This chemical can be analyzed using spectroscopy, enzymatic reactions, or laser ablation. It can also be used in analytical chemistry to identify phospholipases and hydroxybenzoic acids.

1-(3-Fluorophenyl)-2-nitropropene is a versatile building block that can be used as a reagent, speciality chemical, or a reaction component. This compound is also useful for the synthesis of complex compounds. 1-(3-Fluorophenyl)-2-nitropropene has been shown to react with various electrophiles, including carbonyl compounds and nitro compounds, to give substituted products. This chemical is classified as a high quality compound and can be used in the synthesis of pharmaceuticals and other fine chemicals.

Please enquire for more information about (4-nitrophenyl)-N-(3-(trifluoromethyl)phenyl)formamide 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-Nitro-1-(8-quinolyloxy)-4-(trifluoromethyl)benzene 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-2-(2'-pyridinethio)benzaldehyde 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-(Fluoromethyl)-3-(2-methylphenyl)-6-nitro-3H-quinazolin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ruthenium(III) nitrosyl nitrate, soluble in 10% dilute nitric acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

3-Nitrobenzanilide is an intermediate in the synthesis of a number of pharmaceuticals and pesticides. It is used as an activated reagent to introduce the benzoyl group by reaction with dimethylformamide. 3-Nitrobenzanilide can be prepared from phenylacetonitrile, benzoyl chloride, and ammonia or from nitrobenzene and sodium cyanide. The nature of the nitro group on the benzene ring determines whether the product is a diazo compound or a carbonyl compound. 3-Nitrobenzanilide has been shown to have plant disease control properties via its ability to inhibit plant enzymes such as acetylcholine esterase.

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

Please enquire for more information about Z-His-p-nitro-Phe-Phe-OMe including the price, delivery time and more detailed product information at the technical inquiry form on this page