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  2. Cycloheptane - Wikipedia

    en.wikipedia.org/wiki/Cycloheptane

    Cycloheptane, also known as Suberane, [1] is an organic compound, which belongs to the group of cycloalkanes. The compound can occur in different conformers.

  3. Cycloheptene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptene

    With cycloheptene, the cis-isomer is always assumed but the trans-isomer does also exist.One procedure for the organic synthesis of trans-cycloheptene is by singlet photosensitization of cis-cycloheptene with methyl benzoate and ultraviolet light at −35 °C. [2]

  4. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    The cycloalkanes without side chains (also known as monocycloalkanes) are classified as small (cyclopropane and cyclobutane), common (cyclopentane, cyclohexane, and cycloheptane), medium (cyclooctane through cyclotridecane), and large (all the rest).

  5. Cycloheptanone - Wikipedia

    en.wikipedia.org/wiki/Cycloheptanone

    Cycloheptanone is a precursor to bencyclane, a spasmolytic agent and vasodilator. [4] Pimelic acid is produced by the oxidative cleavage of cycloheptanone. [6] Dicarboxylic acids such as pimelic acid are useful for the preparation of fragrances and certain polymers.

  6. Cycloheptatriene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptatriene

    Cycloheptatriene (CHT) is an organic compound with the formula C 7 H 8.It is a closed ring of seven carbon atoms joined by three double bonds (as the name implies) and four single bonds.

  7. Benzocycloheptene - Wikipedia

    en.wikipedia.org/wiki/Benzocycloheptene

    Benzocycloheptenes are cycloheptenes with additional benzene rings attached. Most have two benzene rings, and are called dibenzocycloheptenes.. Some benzocycloheptenes and substituted benzocycloheptenes have medical uses as antihistamines, anticholinergics, antidepressants, and antiserotonergics.

  8. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    In smaller cycloalkenes, it is expected for the bonds to be greater in length uniformly to account for increased strain, but for example, trans-cycloheptane has varying bond lengths. Also, the vinylic carbons on trans cyclohexanes exhibit longer bond lengths than their respective cis isomer for trans-cycloheptane through trans-cyclononene (7 ...

  9. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide-based reagents used as accelerators for vulcanization. The amine itself is an effective corrosion inhibitor. It has been used as a flushing aid in the printing ink industry. [5]