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The trimethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with three methyl groups (–CH 3) as a substituent. [1] [2] Through their different arrangement, they form three structural isomers with the molecular formula C 9 H 12. They also belong to the group of C 3-benzenes.
2,3,4-Trimethylpentane is a branched alkane. It is one of the isomers of octane. References External links. 2,3,4-Trimethylpentane at environmentalchemistry.com; This ...
2,3,4-trimethyl-1,3-pentadiene.png (170 × 116 pixels, file size: 10 KB, MIME type: image/png) This is a file from the Wikimedia Commons . Information from its description page there is shown below.
2,3,3-Trimethylpentane is a chemical compound in the family of hydrocarbons which has a formula of C 8 H 18. It is an isomer of octane. It has a role as a human metabolite, a bacterial metabolite and a mammalian metabolite. [2] It is an alkane and a volatile organic compound.
1,2,4-Trimethylbenzene, also known as pseudocumene, is an organic compound with the chemical formula C 6 H 3 (CH 3) 3. Classified as an aromatic hydrocarbon, it is a flammable colorless liquid with a strong odor. It is nearly insoluble in water but soluble in organic solvents. It occurs naturally in coal tar and petroleum (about 3%).
Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. The other two isomeric trimethylbenzenes are 1,2,4-trimethylbenzene (pseudocumene) and 1,2,3-trimethylbenzene (hemimellitene).
2,3,3-Trimethylpentane; 2,3,4-Trimethylpentane This page was last edited on 10 January 2019 ...
Triphenylmethane was first synthesized in 1872 by the German chemist August Kekulé and his Dutch student Antoine Paul Nicolas Franchimont (1844–1919) by heating diphenylmercury (Hg(C 6 H 5) 2, Quecksilberdiphenyl) with benzal chloride (C 6 H 5 CHCl 2, Benzylenchlorid).