Methyl 4,6- <i>O</i> -benzylidene-α- <scp>D</scp> -glucopyranoside monohydrate

The title compound, C<sub>14</sub>H<sub>18</sub>O<sub>6</sub>·H<sub>2</sub>O, is a partially protected derivative of d-gluco-pyran-ose. The asymmetric unit contains one sugar molecule and one water molecule of crystallization. Classical hydrogen bonds of the O-H⋯O type form a cooperative set and are observed next to a C-H⋯O(water) contact, connecting the entities of the asymmetric unit into a three-dimensional network.

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IUCrData
Published
2025-11-06
DOI
https://doi.org/10.1107/s2414314625009472
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
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article

Methyl 4,6- O -benzylidene-α- D -glucopyranoside monohydrate

Eric C. Hosten, Richard Betz, Mari Grobbelaar
IUCrData
Carbohydrate Chemistry and Synthesis
article

Methyl 4,6- O -benzylidene-α- D -glucopyranoside monohydrate

Eric C. Hosten, Richard Betz, Mari Grobbelaar
article en

Abstract

The title compound, C<sub>14</sub>H<sub>18</sub>O<sub>6</sub>·H<sub>2</sub>O, is a partially protected derivative of d-gluco-pyran-ose. The asymmetric unit contains one sugar molecule and one water molecule of crystallization. Classical hydrogen bonds of the O-H⋯O type form a cooperative set and are observed next to a C-H⋯O(water) contact, connecting the entities of the asymmetric unit into a three-dimensional network.

IUCrDataVol. 10(11)
Nelson Mandela University (ZA)
Openalex Percentile: Top 75%
Carbohydrate Chemistry and Synthesis
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Methyl 4,6- <i>O</i> -benzylidene-α- <scp>D</scp> -glucopyranoside monohydrate — Eric C. Hosten, Richard Betz, et al. · IUCrData (2025) | TGRS Research Map | TGRS