Unknown

Dataset Information

0

2-(4-Iodo-phen-yl)-5-methyl-3-methyl-sulfinyl-1-benzofuran.


ABSTRACT: The title compound, C(16)H(13)IO(2)S, was prepared by the oxidation of 2-(4-iodo-phen-yl)-5-methyl-3-methyl-sulfanyl-1-benzofuran with 3-chloro-peroxy-benzoic acid. The 4-iodo-phenyl ring makes a dihedral angle of 37.97?(9)° with the plane of the benzofuran fragment, and the O atom and the methyl group of the methyl-sulfinyl substituent lie on opposite sides of this plane. The mol-ecular packing is stabilized by C-H?? inter-actions between H atoms on the 4-iodo-phenyl ring and the benzofuran rings, and by an I?O halogen bond of 3.252?(2)?Å with a nearly linear C-I?O angle of 163.06?(8)°. In addition, the stacked mol-ecules exhibit inversion-related S?O contacts [3.209?(2)?Å] involving the sulfinyl groups.

SUBMITTER: Choi HD 

PROVIDER: S-EPMC2961388 | biostudies-literature | 2008 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

2-(4-Iodo-phen-yl)-5-methyl-3-methyl-sulfinyl-1-benzofuran.

Choi Hong Dae HD   Seo Pil Ja PJ   Son Byeng Wha BW   Lee Uk U  

Acta crystallographica. Section E, Structure reports online 20080510 Pt 6


The title compound, C(16)H(13)IO(2)S, was prepared by the oxidation of 2-(4-iodo-phen-yl)-5-methyl-3-methyl-sulfanyl-1-benzofuran with 3-chloro-peroxy-benzoic acid. The 4-iodo-phenyl ring makes a dihedral angle of 37.97 (9)° with the plane of the benzofuran fragment, and the O atom and the methyl group of the methyl-sulfinyl substituent lie on opposite sides of this plane. The mol-ecular packing is stabilized by C-H⋯π inter-actions between H atoms on the 4-iodo-phenyl ring and the benzofuran rin  ...[more]

Similar Datasets

| S-EPMC2961519 | biostudies-literature
| S-EPMC3007479 | biostudies-literature
| S-EPMC2970055 | biostudies-literature
| S-EPMC3006691 | biostudies-literature
| S-EPMC3050243 | biostudies-literature
| S-EPMC3470334 | biostudies-literature
| S-EPMC2983596 | biostudies-literature
| S-EPMC3007935 | biostudies-literature
| S-EPMC3344167 | biostudies-literature
| S-EPMC3011574 | biostudies-literature