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  2. 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]

  3. 2-Coumaranone - Wikipedia

    en.wikipedia.org/wiki/2-Cumaranone

    2-Coumaranone (sometimes also called 2-Cumaranone [3]) is a bicyclic heteroaromatic compound in which a six-membered benzene ring is annulated with a five-membered γ-butyrolactone ring. The 2(3 H )-benzofuranone can also be considered as a lactone of (2-hydroxyphenyl)acetic acid .

  4. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is an organic compound, belonging to the aliphatic amine class. It is a colorless liquid, although, like many amines, samples are often colored due to contaminants.

  5. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    The reaction is highly stereospecific in the sense that the double bond stereochemistry is generally transferred to the relative configuration of the epoxide with essentially perfect fidelity, so that a trans-olefin leads to the stereoselective formation of the trans-2,3-substituted epoxide only, as illustrated by the example above, while a cis ...

  6. Enoyl CoA isomerase - Wikipedia

    en.wikipedia.org/wiki/Enoyl_CoA_isomerase

    Enoyl-CoA-(∆) isomerase (EC 5.3.3.8, also known as dodecenoyl-CoA-(∆) isomerase, 3,2-trans-enoyl-CoA isomerase, ∆3(cis),∆2(trans)-enoyl-CoA isomerase, or acetylene-allene isomerase, [1] is an enzyme that catalyzes the conversion of cis- or trans-double bonds of coenzyme A (CoA) bound fatty acids at gamma-carbon (position 3) to trans double bonds at beta-carbon (position 2) as below:

  7. 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] The double bond in the trans isomer is very strained. [3]

  8. 4,4'-Diaminodicyclohexylmethane - Wikipedia

    en.wikipedia.org/wiki/4,4...

    4,4'-Diaminodicyclohexylmethane is the name for organic compounds with the formula CH 2 (C 6 H 10 NH 2) 2. It is classified as a diamine. In the epoxy industry it is often referred to as PACM, short for para-diamino­dicyclohexyl­methane. It is used as a curing agent for epoxy resins [1] It finds particular use in epoxy flooring. [2]

  9. (1R,3R)-1,2,3-Trimethylcyclopentane - Wikipedia

    en.wikipedia.org/wiki/(1R,3R)-1,2,3-trimethylcyc...

    Because (1R,3R)-1,2,3-trimethylcyclopentane is a cycloalkane, its three methyl substituents are capable of exhibiting cis/trans isomerism. This implies that the methyl groups in positions 1,2, and 3 may occupy different spatial arrangements (i.e.they may either lay cis or trans with respect to each other).