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  2. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    Chemical formula. C 6 H 12 S: Molar mass: 116.22 g·mol −1 ... Cyclohexanethiol is a thiol with the formula C 6 H 11 SH. It is a colorless liquid with a strong odor ...

  3. 4-Vinylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/4-Vinylcyclohexene

    It is produced by buta-1,3-diene dimerization in a Diels-Alder reaction. [5] [4] The reaction is conducted at 110 - 425 °C at pressures of 1.3 - 100 MPa in the presence of a catalyst.

  4. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...

  5. Cyclohexylbenzene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylbenzene

    Cyclohexylbenzene is the organic compound with the structural formula C 6 H 5 −C 6 H 11. It is a derivative of benzene with a cyclohexyl substituent (C 6 H 11 ). It is a colorless liquid.

  6. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]

  7. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...

  8. Benzyl mercaptan - Wikipedia

    en.wikipedia.org/wiki/Benzyl_mercaptan

    Benzyl mercaptan can be prepared by the reaction of benzyl chloride and thiourea. The initially formed isothiouronium salt must be subjected to alkaline hydrolysis to obtain the thiol. It has been identified in boxwood (Buxus sempervirens L.) and is known to contribute to the smoky aroma of certain wines. [2] It also occurs naturally in coffee.

  9. C2H6S - Wikipedia

    en.wikipedia.org/wiki/C2H6S

    The molecular formula C 2 H 6 S (molar mass: 62.13 g/mol, exact mass: 62.0190 u) may refer to: Dimethyl sulfide (DMS), or methylthiomethane Ethanethiol , or ethyl mercaptan