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  2. Cyclohexanedimethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedimethanol

    The reaction conducted in two steps beginning with the conversion of DMT to the diester dimethyl 1,4-cyclohexanedicarboxylate (DMCD): C 6 H 4 (CO 2 CH 3) 2 + 3 H 2 → C 6 H 10 (CO 2 CH 3) 2. In the second step DMCD is further hydrogenated to CHDM: C 6 H 10 (CO 2 CH 3) 2 + 4 H 2 → C 6 H 10 (CH 2 OH) 2 + 2 CH 3 OH. A copper chromite catalyst ...

  3. 1,4-Cyclohexanedimethanol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedimethanol...

    1,4-Cyclohexanedimethanol diglycidyl ether is an organic chemical in the glycidyl ether family. [2] Its formula is C 14 H 24 O 4 and the IUPAC name is 2-[[4-(oxiran-2-ylmethoxymethyl)cyclohexyl]methoxymethyl]oxirane. It has the CAS number of 14228-73-0 [3] and is REACH registered in Europe. [4]

  4. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    [1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 Cl 2 or CCl 4). The product is a vicinal dihalide. This type of reaction is a halogenation and an electrophilic addition.

  5. 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.

  6. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Bromine monochloride (BrCl), a red-brown gas, quite readily dissociates reversibly into bromine and chlorine at room temperature and thus also cannot be obtained pure, though it can be made by the reversible direct reaction of its elements in the gas phase or in carbon tetrachloride. [4] Bromine monofluoride in ethanol readily leads to the ...

  7. Reductions with hydrosilanes - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_hydrosilanes

    Reductions with hydrosilanes are methods used for hydrogenation and hydrogenolysis of organic compounds.The approach is a subset of ionic hydrogenation.In this particular method, the substrate is treated with a hydrosilane and auxiliary reagent, often a strong acid, resulting in formal transfer of hydride from silicon to carbon. [1]

  8. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    It is a cyclohexane ring functionalized with an alcohol, specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow. The compound is a colorless liquid, although commercial samples can appear yellow.

  9. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [ 2 ] ), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide ), leading to a very good approximation of colloidal hard sphere . [ 3 ]