Nitro

2,6-Dinitrobenzaldehyde is a synthetic compound that has been used in the synthesis of other organic compounds and as a reagent for chemical studies. It is a white solid that is soluble in water and alcohols. The compound can be synthesized from 2,6-dichlorobenzaldehyde by nitration followed by reduction. 2,6-Dinitrobenzaldehyde is not radioactive. It has been shown to inhibit the growth of typhimurium at concentrations of 3mg/mL or higher, but not at lower concentrations. This inhibition may be due to its ability to react with the c-h bonds on proteins and nucleic acids. 2,6-Dinitrobenzaldehyde also inhibits the growth of Salmonella enterica serovar Typhimurium ATCC 14028 at high concentrations (3 mg/mL) but not at lower concentrations (0.1 mg/mL).

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4-Nitrophenylmorpholine is a synthetic compound that is derived from morpholine and 4-nitrophenol. It has been shown to be an effective catalyst for the catalytic reduction of nitro groups, which are commonly found in organic solvents. 4-Nitrophenylmorpholine has also been used as a reagent in the synthesis of copper complexes with aryl halides. The reaction time between 4-nitrophenylmorpholine and copper bromide can be controlled by varying the concentration of the reactants. The dihedral angle between the two molecules can also affect the rate of reaction. This material is a clear liquid at room temperature, with a boiling point of 128°C and melting point of -103°C.

1-Bromo-2-nitrobenzene is a chemical compound that can be used as a palladium catalyst for the synthesis of organic compounds. It is a group P2 ligand, which means it will bind to metals such as palladium and platinum. 1-Bromo-2-nitrobenzene undergoes nucleophilic addition reactions with diazonium salts to form the corresponding diazonium bromide. The diazonium bromide can then undergo transfer reactions with other molecules, such as alcohols and amines, to form new products. 1-Bromo-2-nitrobenzene also undergoes staudinger reduction to form a ketone or an aldehyde. This reaction requires the presence of hydrochloric acid, halides, or other electron-donating compounds in order to work properly. Chemical reactions involving 1-bromo-2-nitrobenzene may include

4-Nitro-trans-cinnamonitrile is a synthetic compound that is used in the synthesis of acrylonitrile. It can also be used as a ligand for transition metal complexes, and has a chromophore that absorbs at 270 nm. The different isomers of 4-nitro-trans-cinnamonitrile have been shown to have ambident properties, which means they can act as both an acid and a base. This property makes it useful in catalytic reactions.

o-Nitrochlorobenzene is a chemical that belongs to the nitro group of compounds. It is used in the synthesis of various other chemicals, such as pharmaceuticals and dyes. o-Nitrochlorobenzene has been shown to be toxic to rats at higher doses, with evidence of toxicity including cavity formation and low energy levels. The long-term effects of o-nitrochlorobenzene are not well understood. There is also not enough information on its carcinogenicity in animals or humans.

Applications 4-Nitrobenzenesulfonamide (cas# 6325-93-5) is a useful research chemical.