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  2. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Molar mass: 121.139 g·mol −1 Appearance Off-white solid Density: 1.341 g/cm 3: Melting point: ... Benzamide is an organic compound with the chemical formula of C 7 ...

  3. C7H7NO - Wikipedia

    en.wikipedia.org/wiki/C7H7NO

    The molecular formula C 7 H 7 NO (molar mass: 121.14 g/mol, exact mass: 121.0528 u) may refer to: 2-Acetylpyridine; 2-Aminobenzaldehyde; Benzamide; Formanilide

  4. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Molar mass: 122.123 g/mol ... Std molar entropy (S ⦵ 298) 167. ... benzonitrile and benzamide can be hydrolyzed to benzoic acid or its conjugate base in acid or ...

  5. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.

  6. 3-Aminobenzamide - Wikipedia

    en.wikipedia.org/wiki/3-aminobenzamide

    Molar mass: 136.154 g·mol −1 Appearance Off-white powder Density: ... 3-Aminobenzamide is a benzamide. It is an off-white powder and has the chemical formula C 7 H ...

  7. Benzamidine - Wikipedia

    en.wikipedia.org/wiki/Benzamidine

    Benzamidine is a reversible competitive inhibitor of trypsin, trypsin-like enzymes, and serine proteases. [4]It is often used as a ligand in protein crystallography to prevent proteases from degrading a protein of interest.

  8. 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.

  9. Benzaldehyde oxime - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde_oxime

    Benzaldehyde oxime undergoes Beckmann rearrangement to form benzamide, catalyzed by nickel salts [3] or photocatalyzed by BODIPY. [4] Its dehydration yields benzonitrile.It can be hydrolyzed to regenerate benzaldehyde.