( RS )‐Benzyl mandelate | Zendy

Mughal Robila K. | Zendy; Pritchard Robin G. | Zendy; Davey Roger J. | Zendy

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( RS )‐Benzyl mandelate

Author(s) -

Mughal Robila K.,

Pritchard Robin G.,

Davey Roger J.

Publication year - 2004

Publication title -

acta crystallographica section e

Language(s) - English

Resource type - Journals

ISSN - 1600-5368

DOI - 10.1107/s1600536804025024

Subject(s) - mandelic acid , benzyl alcohol , crystallization , hydrogen bond , intermolecular force , chemistry , chirality (physics) , alcohol , crystallography , stereochemistry , medicinal chemistry , organic chemistry , catalysis , molecule , chiral symmetry , physics , quantum mechanics , nambu–jona lasinio model , quark

A benzyl ester of mandelic acid, C 15 H 14 O 3 , was obtained by the crystallization of racemic mandelic acid from benzyl alcohol followed by vacuum drying at 363 K. The structure is composed of two hydrogen‐bonded chains of S or R configuration, running along the shortest crystallographic b axis. There is one molecule in the asymmetric unit and each molecule forms four intermolecular hydrogen bonds with two other molecules of the same chirality.

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