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3-Nitrobenzaldehyde is an organic compound with the formula O 2 NC 6 H 4 CHO. It is one of three isomers of nitrobenzaldehyde. It contains a nitro group meta-substituted to the aldehyde. 3-Nitrobenzaldehyde is the primary product obtained via the mono-nitration of benzaldehyde with nitric acid. [3] C 6 H 5 CHO + HNO 3 → O 2 NC 6 H 4 CHO + H 2 O
3-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is an aromatic compound and under standard conditions, it is an off-white solid. The two substituents are in a meta position with respect to each other, giving the alternative name of m-nitrobenzoic acid.
2-Methylbenzaldehyde is an organic compound with the formula CH 3 C 6 H 4 CHO. It is a colorless liquid. [1] Use and occurrence. Of its many reactions, 2 ...
CH 3 CH 2 NH 2: ethylamine: 75-04-7 C 2 H 6 O 2: ethylene glycol: 107-21-1 HCOOH: formic acid: 64-18-6 C 5 H 6 O 2: furfuryl alcohol: 98-00-0 C 3 H 8 O 3: glycerol: 56-81-5 CH 3 OH: methanol: 67-56-1 CH 3 N(C 2 H 4 OH) 2: methyl diethanolamine: 105-59-9 CH 3 NC: methyl isocyanide: 593-75-9 C 5 H 9 NO: N-Methyl-2-pyrrolidone: 872-50-4 CH 3 CH 2 ...
c 6 h 5 no 2 + 3 h 2 → c 6 h 5 nh 2 + 2 h 2 o Aniline is a precursor to urethane polymers, rubber chemicals, pesticides , dyes (particularly azo dyes ), explosives , and pharmaceuticals . Most aniline is consumed in the production of methylenedianiline , a precursor to polyurethanes.
3-Nitrobenzoic acid is a precursor to 3-aminobenzoic acid, which in turn is used to prepare some dyes. It can be prepared by nitration of benzoic acid. It also can be prepared by treating benzaldehyde under nitration conditions, a process that initially converts the aldehyde to the acid.
2-Nitrobenzaldehyde is an intermediate in an early route to indigo, a water-insoluble dye commonly used to dye jeans and other fabrics.In the Baeyer-Drewson indigo synthesis, 2-nitrobenzaldehyde condenses with acetone in basic aqueous solution to yield indigo in a one-pot synthesis [9] [10] The method was abandoned in the early part of the 20th century, being replaced by routes from aniline.
The molecular formula C 7 H 5 NO 3 (molar mass: 151.12 g/mol, exact mass: 151.0269 u) may refer to: 2-Nitrobenzaldehyde; 3-Nitrobenzaldehyde;