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4-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 para-substituted to an aldehyde. 4-Nitrobenzaldehyde is obtained by oxidation of 4-nitrotoluene or hydrolysis of 4-nitrobenzalbromide: [3] O 2 NC 6 H 4 CHBr 2 + H 2 O → O 2 NC 6 H 4 CHO + 2 HBr
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; 4-Nitrobenzaldehyde
Nitrobenzaldehyde may refer to any of the three isomeric chemical compounds : 2-Nitrobenzaldehyde; 3-Nitrobenzaldehyde; 4-Nitrobenzaldehyde; isomers of ...
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
C 7 H 5 Br O: Molar mass: 185.020 g·mol −1 Appearance colorless liquid. Density: 1.587 g/mL [1] Melting point: 18 to 21 °C (64 to 70 °F; 291 to 294 K) [1] Boiling point: 233 to 236 °C (451 to 457 °F; 506 to 509 K) [1] Hazards GHS labelling:
4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula BrC 6 H 4 CHO. It is one of three isomers of bromobenzaldehyde . [ 3 ] It displays reactivity characteristic of benzaldehyde and an aryl bromide .
Benzaldehyde (C 6 H 5 CHO) is an organic compound consisting of a benzene ring with a formyl substituent. It is among the simplest aromatic aldehydes and one of the most industrially useful. It is a colorless liquid with a characteristic almond -like odor , and is commonly used in cherry -flavored sodas . [ 5 ]
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.