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tetramethylbenzenes

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Also known as tetramethylbenzene

The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH3) as a substituent. Through their different arrangement, they form three structural isomers with the molecular formula C10H14. They also belong to the group of C4-benzenes. The best-known isomer is durene.

In the Vinony graph

Within Vinony's link graph, tetramethylbenzenes is referenced by 104 other articles, and connects out to benzene, aromatic compound and pentene.

Vinony files it under Alkylbenzenes and C4-Benzenes.

Its subject is documented across 8 Wikipedia language editions.

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Tetramethylbenzenes

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The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH3) as a substituent. Through their different arrangement, they form three structural isomers with the molecular formula C10H14. They also belong to the group of C4-benzenes. The best-known isomer is durene. {| class="wikitable" style="text-align:center; font-size:90%" |- | class="hintergrundfarbe6" colspan="4" | Tetramethylbenzenes |- | class="hintergrundfarbe5" align="left" | Common name |prehnitene||isodurene||durene |- | class="hintergrundfarbe5" align="left" | Systematic name | 1,2,3,4-tetramethylbenzene || 1,2,3,5-tetramethylbenzene || 1,2,4,5-tetramethylbenzene |- | class="hintergrundfarbe5" align="left" | Structural formula | 80px || 120px || 120px |- | class="hintergrundfarbe5" align="left" | CAS Registry Number | 488-23-3 || 527-53-7 || 95-93-2 |}

==References==

Excerpted from Wikipedia’s “tetramethylbenzenes” article, available under the CC BY-SA 4.0 licence.

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