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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 ]

  3. C7H7NO - Wikipedia

    en.wikipedia.org/wiki/C7H7NO

    Upload file; Search. Search. ... Download as PDF; Printable version ... The molecular formula C 7 H 7 NO (molar mass: 121.14 g/mol, exact mass: 121.0528 u) may ...

  4. 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.

  5. 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.

  6. 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.

  7. C7H15N - Wikipedia

    en.wikipedia.org/wiki/C7H15N

    Upload file; Search. ... Download as PDF; ... Appearance. move to sidebar hide. The molecular formula C 7 H 15 N (molar mass: 113. 20 g/mol, exact mass ...

  8. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    In this prototypical example involving benzophenone, the tetrahedral intermediate expels phenyl anion to give benzamide and benzene as the organic products. Benzophenone is a common photosensitizer in photochemistry. It crosses from the S 1 state into the triplet state with nearly 100% yield.

  9. Benzophenone imine - Wikipedia

    en.wikipedia.org/wiki/Benzophenone_imine

    Benzophenone imine can be prepared by the thermal decomposition of benzophenone oxime: [2]. 2 (C 6 H 5) 2 C=NOH → (C 6 H 5) 2 C=NH + (C 6 H 5) 2 C=O. Benzophenone imine can also be synthesized by addition of phenylmagnesium bromide to benzonitrile followed by careful hydrolysis (lest the imine be hydrolyzed): [3]