![[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]](rz2297contents.gif)
Acta Cryst. (2009). E65, o679 [ doi:10.1107/S1600536809007260 ]
-D-allopyranosyloxy)benzylidene]thiosemicarbazideAbstract: The title compound, C22H27N3O10S, was synthesized by reaction of an ethanol solution of helicid (systematic name: 4-formylphenl-
-D-allopyranoside), thiosemicarbazide and acetic acid. The molecule exhibits a trans conformation with respect to the C=N double bond. The pyran ring adopts a chair conformation. In the crystal structure, the molecules are linked into chains parallel to the b axis by intermolecular N-H
O hydrogen bonds.
Online 6 March 2009
Copyright © International Union of Crystallography
IUCr Webmaster