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  2. Benzaldehyde oxime - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde_oxime

    Benzaldehyde oxime is an organic compound with the formula C 7 H 7 NO. Benzaldehyde oxime can be synthesized from benzaldehyde and hydroxylamine hydrochloride in presence of a base. The reaction at room temperature in methanol gives 9% E -isomer and 82% Z -isomer.

  3. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.

  4. 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 ]

  5. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen. The benzoyl group has a mass of 105 amu. The term "benzoyl" should not be confused with benzyl, which has the formula − ...

  6. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3,4,5-Trimethoxybenzaldehyde

    Download as PDF; Printable version; ... 3,4,5-Trimethoxy benzaldehyde. Identifiers CAS Number. 86-81-7 ... Chemical formula. C 10 H 12 O 4: Molar mass:

  7. 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.

  8. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    Bromobenzaldehydes are any of three organic compounds with the formula BrC 6 H 4 COH, consisting of a formyl group and a bromine atom attached to a central benzene ring. They can be considered as brominated derivatives of benzaldehyde , or as formylated derivatives of bromobenzene .

  9. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.