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  2. 1,3-Dichloropropene - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropene

    1.217 g/mL (cis); 1.224 g/mL (trans) Melting point: ... 1,3-Dichloropropene, sold under diverse trade names, is an organochlorine compound with the formula C 3 H 4 Cl ...

  3. 1,2-Dichloroethylene - Wikipedia

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

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2. The two compounds are isomers, each being colorless liquids with a sweet odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...

  4. Kurnakov test - Wikipedia

    en.wikipedia.org/wiki/Kurnakov_test

    The Kurnakov test, also known as Kurnakov's reaction, is a chemical test that distinguishes pairs of cis- and trans-isomers of [PtA 2 X 2] (A = NH 3, X = halogen or pseudohalide). Upon treatment with thiourea , the trans -dihalides give less soluble white products, whereas the cis -dihalides give more soluble yellow products.

  5. 1,2-Dichloropropane - Wikipedia

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

    1,2-Dichloropropane is an intermediate in the production of perchloroethylene and other chlorinated chemicals. [4] It was once used as a soil fumigant , chemical intermediate, as well as an industrial solvent and was found in paint strippers, varnishes, and furniture finish removers but some of these uses have been discontinued.

  6. 1,3-Dichloropropane - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropane

    1,3-Dichloropropane is a compound of chlorine, hydrogen, and carbon. It may be found as a contaminant in soil fumigants containing 1,3-dichloropropene . [ 2 ] It has low acute toxicity.

  7. (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).

  8. Descriptor (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Descriptor_(Chemistry)

    All-cis 1,2,3-trichlorocyclopentane The descriptors ( r ) and ( s ) are used to describe the absolute configuration of pseudoasymmetric centers. [ 38 ] Pseudoasymmetry occurs when four different substituents are attached to one carbon atom, two of which differ only by their absolute stereochemical configuration.

  9. 1,3-Dichloropropan-2-ol - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropan-2-ol

    [2] [3] 1,3-DCP is a believed to be a carcinogen and mutagen. [4] The International Agency for Research on Cancer classifies it as a Group 2B carcinogen ("possibly carcinogenic to humans"). [5] Along with 3-monochloropropane-1,2-diol (3-MCPD), 1,3-DCP is found in some Asian style sauces such as soy sauce and oyster sauce. [6] [7] [8]