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  2. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Benzamide is an organic compound with the chemical formula of C 7 H 7 NO. It is the simplest amide derivative of benzoic acid. In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals. [5] It is slightly soluble in water, [2] and soluble in many organic solvents. [6]

  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. Benzamidine - Wikipedia

    en.wikipedia.org/wiki/Benzamidine

    Benzamidine is an organic compound with the formula C 6 H 5 C(NH)NH 2. It is the simplest aryl amidine. The compound is a white solid that is slightly soluble in water. It is usually handled as the hydrochloride salt, a white, water-soluble solid. [2]

  5. 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.

  6. Ammonium benzoate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_benzoate

    C 7 H 9 N O 2: Molar mass: 139.15 g/mol Appearance White solid Density: 1.26 g/cm 3: ... Ammonium benzoate can be dehydrated to form benzamide. References

  7. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    ɪ k /) is a white (or colorless) solid organic compound with the formula C 6 H 5 COOH, whose structure consists of a benzene ring (C 6 H 6) with a carboxyl (−C(=O)OH) substituent. The benzoyl group is often abbreviated "Bz" (not to be confused with "Bn," which is used for benzyl ), thus benzoic acid is also denoted as BzOH, since the benzoyl ...

  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. Benzimidazole - Wikipedia

    en.wikipedia.org/wiki/Benzimidazole

    Benzimidazole is a base: . C 6 H 4 N(NH)CH + H + → [C 6 H 4 (NH) 2 CH] +. It can also be deprotonated with stronger bases: . C 6 H 4 N(NH)CH + LiH → Li [C 6 H 4 N 2 CH] + H 2. The imine can be alkylated and also serves as a ligand in coordination chemistry.

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