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In the context of organic molecules, aryl refers to any functional group or substituent derived from a simple aromatic ring, may it be phenyl, thiophene, indolyl, etc (see IUPAC nomenclature) [1]. "Aryl" is used for the sake of abbreviation or generalization.

A simple aryl group is phenyl, C6H5; it is derived from benzene. The tolyl group, CH3C6H4, is derived from toluene (methylbenzene). The xylyl group, (CH3)2C6H3, is derived from xylene (dimethylbenzene).

A few different types of benzene derived aryl groups. From left to right: phenyl, benzyl, tolyl, o-xylyl.

Biaryls may display axial chirality. Arylation is simply any chemical process in which an aryl group is attached to a substrate.

[edit] See also

[edit] References

  1. ^ http://goldbook.iupac.org/A00464.html
  2. ^ Bock KW, Köhle C (2006). "Ah receptor: dioxin-mediated toxic responses as hints to deregulated physiologic functions". Biochem. Pharmacol. 72 (4): 393–404. doi:10.1016/j.bcp.2006.01.017. PMID 16545780. 



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