Skip to content
EntityQ2406753· pop 9· linked from 104 articles

tetramethylbenzenes

Sign in to save

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.

Wikidata facts

Show 1 more fact
Commons category
Tetramethylbenzenes

via Wikidata · CC0

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

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.

Available in 8 languages

via Wikidata sitelinks · CC0