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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 Appearance Colorless liquid Density: 0.95 g/cm 3: Boiling point: 158 to 160 °C (316 to 320 °F; 431 to ...

  3. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is produced by the partial hydrogenation of benzene, a process developed by the Asahi Chemical company. [4] The main product of the process is cyclohexane because cyclohexene is more easily hydrogenated than benzene. In the laboratory, it can be prepared by dehydration of cyclohexanol. [5] C 6 H 11 OH → C 6 H 10 + H 2 O

  4. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    An acyclic alkyl has the general formula of −C n H 2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H 2n−1. [2] Typically an alkyl is a part of a larger molecule. In structural formulae, the symbol R is used to designate a generic (unspecified) alkyl group.

  5. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a cycloalkane with the molecular formula C 6 H 12.Cyclohexane is non-polar.Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used).

  6. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is the organic compound with the formula HOCH(CH 2) 5.The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature.

  7. 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

  8. 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.

  9. 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.