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  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Molar mass: 84.162 g·mol −1 Appearance Colourless liquid Odor: Sweet, gasoline-like Density: ... Cyclohexane is a cycloalkane with the molecular formula C 6 H 12.

  3. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Standard molar entropy, S o liquid: 204 J/(mol K) Enthalpy of combustion, ... log 10 of Cyclohexane vapor pressure. Uses formula: ...

  4. 1,2-Diaminocyclohexane - Wikipedia

    en.wikipedia.org/wiki/1,2-Diaminocyclohexane

    The product is an epoxy curing agent for use in Coatings, Adhesives, Sealants and Elastomers - CASE. [2] It is particularly useful in epoxy flooring. [3] It may also be reacted with diethyl maleate utilizing the Michael reaction to produce a polyaspartic compound of CAS number 481040-92-0. [4]

  5. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    Molar mass: 128.171 g·mol −1 Appearance white solid Density: 1.0274 g/cm 3: Melting point: ... It is the carboxylic acid of cyclohexane. It is a colorless oil that ...

  6. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.

  7. Cyclohexanehexone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanehexone

    Molar mass: 168.060 g·mol −1 Except where otherwise noted, data are given for materials in their standard state ... the sixfold ketone of cyclohexane.

  8. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    Molar mass: 163.06 g/mol Appearance colorless liquid Density: ... Bromocyclohexane can be prepared by the free radical bromination of cyclohexane. Safety

  9. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is most stable in a half-chair conformation, [11] unlike the preference for a chair form of cyclohexane. One basis for the cyclohexane conformational preference for a chair is that it allows each bond of the ring to adopt a staggered conformation. For cyclohexene, however, the alkene is planar, equivalent to an eclipsed conformation ...