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E-[4-(?-d-Allopyranos-yloxy)phen-yl]-1-(4-chloro-phen-yl)prop-2-enone ethanol solvate.


ABSTRACT: The title compound, C(21)H(21)ClO(7)·C(2)H(5)OH was synthesized by the condensation reaction between helicid [systematic name: 4-(?-d-allopyranos-yloxy)benzaldehyde] and 4-chloro-aceto-phen-one in ethanol. In the mol-ecular structure, the pyran-oside ring adopts a chair conformation. In the crystal structure, the molecules are linked by inter-molecular O-H?O hydrogen bonds involving the OH groups from the pyran-oside unit and from the ethanol solvent mol-ecule.

SUBMITTER: Yang CL 

PROVIDER: S-EPMC2968659 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

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E-[4-(β-d-Allopyranos-yloxy)phen-yl]-1-(4-chloro-phen-yl)prop-2-enone ethanol solvate.

Yang Cong-Ling CL   Luo Hua-Ling HL   Yin Xiu-Juan XJ   Li Ying Y   Yin Shu-Fan SF  

Acta crystallographica. Section E, Structure reports online 20090228 Pt 3


The title compound, C(21)H(21)ClO(7)·C(2)H(5)OH was synthesized by the condensation reaction between helicid [systematic name: 4-(β-d-allopyranos-yloxy)benzaldehyde] and 4-chloro-aceto-phen-one in ethanol. In the mol-ecular structure, the pyran-oside ring adopts a chair conformation. In the crystal structure, the molecules are linked by inter-molecular O-H⋯O hydrogen bonds involving the OH groups from the pyran-oside unit and from the ethanol solvent mol-ecule. ...[more]

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