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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.
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[2] As of early 1990s, it was present in American [3] and European [4] gasoline in small amounts, and by 2011 its share in US gasoline varied between 1 and 3%. [5] It has a research octane number of 103 and motor octane number of 95. [6] The C 6 core of methylcyclopentane is not perfectly planar and can pucker to alleviate stress in its ...
Cyclopentane is a minor component of automobile fuel, with its share in US gasoline varying between 0.2 and 1.6% in early 1990s [8] and 0.1 to 1.7% in 2011. [9] Its research and motor octane numbers are reported as 101 or 103 and 85 or 86 respectively. [10] [11]
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.
2,4-Dimethylpentane; 3,3-Dimethylpentane This page was last edited on 17 March 2021, at 16:47 (UTC). Text is available under the Creative Commons Attribution ...
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Examples include 2-pentyl- and 2-heptylcyclopentanone. [4] It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. [5] Cyclopentobarbital, a drug made from cyclopentanone. Cyclopentanone is also used to make cyclopentamine, the pesticide pencycuron, and pentethylcyclanone. [5]