Nitro

4-Nitrophenyl propionate is a synthetic surfactant that is used in many products, including detergents, fabric softeners, and dishwashing liquids. It has been shown to have a positioning effect on the enzyme lipase and to shift its enzymatic activity. 4-Nitrophenyl propionate can be used as a catalyst for sodium fusidate in the synthesis of microemulsions. The catalytic activity of 4-nitrophenyl propionate is constant and it has high catalytic efficiency.

4-Bromo-3-nitroaniline is a white crystalline solid. It has a molecular weight of 256.38 and it has a molar mass of 314.6 g/mol. This chemical belongs to the group of aromatic compounds, which are organic compounds that contain at least one benzene ring, and are often used in the production of dyes and perfumes. 4-Bromo-3-nitroaniline can be synthesized by nitrating an aromatic compound containing an amino group, such as 1,4-diaminobenzene (1). Nitration is the process whereby nitric acid reacts with an organic compound to produce nitrates, which can be further reacted to produce a variety of other organic molecules with different properties. The molecular structure of 4-bromo-3-nitroaniline consists of two methyl groups (-CH3) bonded to each end of the molecule's central carbon atom (-C),

1-(4-Chlorophenyl)-2-nitropropene is a versatile building block that can be used in the synthesis of a variety of compounds. It is an aromatic compound with a molecular weight of 122.1 and chemical formula CHClNO. It has a melting point of -44°C, boiling point of 166°C, and density at 20°C of 1.11 g/mL. This product has also been shown to be useful as an intermediate or reaction component for the synthesis of polymers, pharmaceuticals, pesticides, and other organic compounds. 1-(4-Chlorophenyl)-2-nitropropene is soluble in water (10 mg/mL) and alcohols (10 mg/mL). This product is classified as not hazardous according to the Globally Harmonized System (GHS) criteria for classification and labeling of chemicals.

1-(Phenyl) 2-nitroethane is a nitro compound that reacts with hydroxyl groups in the body to produce reactive oxygen species. The nitro group on the 1-position of the benzoic acid moiety is converted to an amino group, which is oxidized to form a nitrite ion. Reactive oxygen species are generated from the reaction of 1-(phenyl) 2-nitroethane with hydrogen peroxide and superoxide radicals. 1-(Phenyl) 2-nitroethane has been shown to have antinociceptive properties, as well as minimal toxicity when used in rats at concentrations between 10 and 100 mg/kg. It has also been shown to be a natural product that can induce apoptosis by disrupting mitochondrial membrane potential and reducing intracellular calcium levels. Multiple molecular docking analysis studies have also shown that 1-(phenyl) 2-nitroethane binds to human cytochrome P450 enzyme CYP

P-Nitrobenzoic acid is a nitro compound that is used as an intermediate in the synthesis of various pharmaceuticals. It is also used in wastewater treatment to remove protocatechuic acid, which is produced during the oxidation of phenols by peroxidase. P-Nitrobenzoic acid can be synthesized by reacting sodium nitrite with p-hydroxybenzoic acid. The structure of this compound was determined through a series of experiments, and it was found that it has two nitrogen atoms that are incorporated into the benzene ring. This compound reacts with aziridine in an exothermic reaction mechanism to form an unstable five membered ring. This reaction proceeds through a series of steps and eventually forms p-nitrobenzoic acid.