![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[Supplementary Material]](/e/graphics/supplementarymaterialsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Open access]](/e/graphics/free.gif)
![[Contents scheme]](bg2430contents.gif)
Acta Cryst. (2012). E68, o58 [ doi:10.1107/S1600536811052160 ]
Abstract: The title compound, C13H13BrO3S, was prepared by alkaline hydrolysis of ethyl 2-(5-bromo-3-isopropylsulfanyl-1-benzofuran-2-yl)acetate. In the crystal, the carboxyl groups are involved in intermolecular O-H
O hydrogen bonds, which link the molecules into dimers. These dimers are further packed into stacks along the c axis by intermolecular C-H
interactions, and by slipped
-
interactions between the furan rings of adjacent molecules [centroid-centroid distance = 3.472 (2) Å, interplanar distance = 3.398 (2) Å and slippage = 0.713 (2) Å].
Online 10 December 2011
Copyright © International Union of Crystallography
IUCr Webmaster