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2-Phenyl-ethyl 1-thio-?-d-galactopyran-oside hemihydrate.


ABSTRACT: The title compound, C(14)H(20)O(5)S·0.5H(2)O, crystallizes with two organic mol-ecules and a solvent water mol-ecule in the asymmetric unit. In both mol-ecules, the hexa-pyranosyl rings adopt a slightly distorted chair conformation ((5)C(2)) with four substituents in equatorial positions and one substituent in an axial position. The main difference between the organic mol-ecules is the dihedral angle between the phenyl ring and the best plane defined by the O-C(1)-C(2)-C(3) atoms (r.m.s deviations = 0.003 and 0.043?Å) of the hexa-pyranosyl rings [47.4?(4) and 86.5?(4)°]. In the asymmetric unit, mol-ecules are linked by two strong O-H?O hydrogen bonds. In the crystal, the components are linked by a total of 10 distinct O-H?O hydrogen bonds, resulting in the formation of a two-dimensional network parallel to the ab plane.

SUBMITTER: Brito I 

PROVIDER: S-EPMC3200876 | biostudies-other | 2011 Sep

REPOSITORIES: biostudies-other

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2-Phenyl-ethyl 1-thio-β-d-galactopyran-oside hemihydrate.

Brito Iván I   Szilágyi László L   Kumar Ambati Ashok AA   Albanez Joselyn J   Bolte Michael M  

Acta crystallographica. Section E, Structure reports online 20110811 Pt 9


The title compound, C(14)H(20)O(5)S·0.5H(2)O, crystallizes with two organic mol-ecules and a solvent water mol-ecule in the asymmetric unit. In both mol-ecules, the hexa-pyranosyl rings adopt a slightly distorted chair conformation ((5)C(2)) with four substituents in equatorial positions and one substituent in an axial position. The main difference between the organic mol-ecules is the dihedral angle between the phenyl ring and the best plane defined by the O-C(1)-C(2)-C(3) atoms (r.m.s deviatio  ...[more]

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