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  2. 2-Nitrobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Nitrobenzaldehyde

    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.

  3. 3-Nitrobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3-nitrobenzaldehyde

    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. Product distribution is about 19% for the ortho-, 72% for the meta- and 9% for the para isomers.

  4. 4-Nitrobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobenzaldehyde

    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.

  5. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    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 ]

  6. β-Nitrostyrene - Wikipedia

    en.wikipedia.org/wiki/Β-Nitrostyrene

    β-Nitrostyrene is a chemical precursor for slimicides and dyes. Specifically bromo-nitrostyrene is obtained upon treatment with bromine followed by partial dehydrohalogenation [2] while 2-nitrobenzaldehyde is obtained by treatment with ozone respectively.

  7. Leuckart reaction - Wikipedia

    en.wikipedia.org/wiki/Leuckart_reaction

    The Leuckart reaction is the chemical reaction that converts aldehydes or ketones to amines. The reaction is an example of reductive amination. [1] The reaction, named after Rudolf Leuckart, uses either ammonium formate or formamide as the nitrogen donor and reducing agent. It requires high temperatures, usually between 120 and 130 °C; for the ...

  8. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  9. Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzoic_acid

    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. 4-Nitrobenzoic acid is a precursor to 4-aminobenzoic acid , which is in turn used to prepare the anesthetic procaine . 4-Nitrobenzoic acid is prepared by ...