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  2. 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 ]

  3. Category:Benzaldehydes - Wikipedia

    en.wikipedia.org/wiki/Category:Benzaldehydes

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  4. Betti reaction - Wikipedia

    en.wikipedia.org/wiki/Betti_reaction

    The original Betti base synthesized from 2-naphthol and the imine produced from the reaction of benzaldehyde and ammonia. The product of the Betti reaction is called the Betti base. The stereochemistry of the base was resolved into two isomers by using tartaric acid. Uses for the Betti base and its derivatives include: [1] [3] [4]

  5. 2-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobenzaldehyde

    It is one of three isomeric monochlorinated benzaldehyde. 3-Chlorobenzaldehyde and 4-chlorobenzaldehyde are the other isomers. Whereas benzaldehyde is prone to autoxidation, the 2-chloro derivatives are more air-stable.

  6. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    They can be considered as brominated derivatives of benzaldehyde, or as formylated derivatives of bromobenzene. Bromobenzaldehyde isomers Common name and systematic name

  7. 2-Carboxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Carboxybenzaldehyde

    2-Carboxybenzaldehyde is a chemical compound.It consists of a benzene ring, with an aldehyde and a carboxylic acid as substituents that are ortho to each other. The compound exhibits ring–chain tautomerism: the two substituents can react with each other to form 3-hydroxyphthalide, a cyclic lactol.

  8. Chalcone - Wikipedia

    en.wikipedia.org/wiki/Chalcone

    Chalcone is usually prepared by an aldol condensation between benzaldehyde and acetophenone. [ 6 ] This reaction, which can be carried out without any solvent, is so reliable that it is often given as an example of green chemistry in undergraduate education.

  9. 4-Hydroxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-hydroxybenzaldehyde

    4‑Hydroxy­benzaldehyde (para‑hydroxy­benzaldehyde) is an organic compound with the formula C 6 H 4 OH(CHO). [ 4 ] [ 5 ] Along with 2-hydroxybenzaldehyde and 3-hydroxybenzaldehyde , it is one of the three isomers of hydroxybenzaldehyde .