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  2. trans-1,2-Diaminocyclohexane - Wikipedia

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

    trans-1,2-Diaminocyclohexane is an organic compound with the formula C 6 H 10 (NH 2) 2. This diamine is a building block for C 2-symmetric ligands that are useful in asymmetric catalysis. [1] A mixture of all three stereoisomers of 1,2-diaminocyclohexane is produced by the hydrogenation of o-phenylenediamine.

  3. 1,2-Diaminocyclohexane - Wikipedia

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

    1,2-Diaminocyclohexane (DACH) is an organic compound with the formula (CH 2) 4 (CHNH 2) 2. It is a mixture of three stereoisomers: cis -1,2-diaminocyclohexane and both enantiomers of trans -1,2-diaminocyclohexane. The mixture is a colorless, corrosive liquid, although older samples can appear yellow. It is often called DCH-99 and also DACH.

  4. Cyclohexane (data page) - Wikipedia

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

    Critical point. 554 K (281 °C), 4070 kPa. Std enthalpy change of fusion, Δ fusH o. 2.68 kJ/mol crystal I → liquid. Std entropy change of fusion, Δ fusS o. 9.57 J/ (mol·K) crystal I → liquid. Std enthalpy change of vaporization, Δ vapH o. 32 kJ/mol. Std entropy change of vaporization, Δ vapS o.

  5. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Methylcyclohexane(cyclohexylmethane) is an organic compoundwith the molecular formula is CH3C6H11. Classified as saturated hydrocarbon, it is a colourless liquidwith a faint odor. Methylcyclohexane is used as a solvent. It is mainly converted in naphtha reformersto toluene.[4]

  6. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH3)2C (CH2)2(CO)2(CH2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  7. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    trans -but-2-ene. Cis–trans isomerism, also known as geometric isomerism, describes certain arrangements of atoms within molecules. The prefixes " cis " and " trans " are from Latin: "this side of" and "the other side of", respectively. [ 1 ] In the context of chemistry, cis indicates that the functional groups (substituents) are on the same ...

  8. 1,2-Dimethylcyclopropane - Wikipedia

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

    1,2-Dimethylcyclopropane is a cycloalkane consisting of a cyclopropane ring substituted with two methyl groups attached to adjacent carbon atoms. [1] It has three stereoisomers, one cis -isomer and a pair of trans - enantiomers, which differ depending on the orientation of the two methyl groups. As with other cyclopropanes, ring tension results ...

  9. Methylenecyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclohexane

    C=C1CCCCC1. Properties. Chemical formula. C 7 H 12. Molar mass. 96.170 g/mol. Boiling point. 102 to 103 °C (216 to 217 °F; 375 to 376 K) Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).