Bring the power of IUPAC naming to your desktop!

ACD/Name (Chemist Version) offers a standardized set of features for quick and simple generation of IUPAC names, and structures from names. It is a streamlined version of our popular ACD/Name software.

View a full description and pricing on our web store.

Heterocyclic Ring Assemblies

Rule B-13

13.1 - Assemblies of two or more identical heterocyclic systems are named by placing the prefix "bi-", "ter-", "quater-", etc., before the name of the heterocyclic system or radical. The numbering of the assembly is that of the corresponding heterocyclic systems, one component being assigned unprimed and the others primed, doubly primed, etc., numbers. The points of attachment are indicated by appropriate locants before the name. Other structural features are described as recorded for hydrocarbon ring assemblies in Rules A-52.1 (double bond between two components), A-52.3 (substituents), A-53.3 (hydrogenation), A-54.1 (numerical prefixes), and A-55.1 and A-56.1 (radicals), insofar as fixed numbering of the heterocyclic system allows.

Examples to Rule B-13.1

2,3'-Bifuran

or 2,3'-Bifuryl

2,2'-Bipyridin-6-yl

or 2,2'-Bipyridyl-6-yl

or 6-(2-Pyridyl)-2-pyridyl

2,2':6',2'':6'',2'''-Quaterpyridine

See Recommendations'93 R-2.4.4


search
This HTML reproduction of Sections A, B and C of IUPAC "Blue Book" is as close as possible to the published version [see Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H, Pergamon Press, Oxford, 1979. Copyright 1979 IUPAC.] If you need to cite these rules please quote this reference as their source.

Published with permission of the IUPAC by Advanced Chemistry Development, Inc., www.acdlabs.com, +1(416)368-3435 tel, +1(416)368-5596 fax. For comments or suggestions please contact webmaster@acdlabs.com