Volume 57, Issue 8 pp. o715-o716

3,4-Di­hydroxy­phenyl­acetic acid

Nobuo Okabe

Nobuo Okabe

Faculty of Pharmaceutical Sciences, Kinki university, Kokawae 3-4-1, Higashiosaka, Osaka 577-8502, Japan

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Hasuyo Kyoyama

Hasuyo Kyoyama

Faculty of Pharmaceutical Sciences, Kinki university, Kokawae 3-4-1, Higashiosaka, Osaka 577-8502, Japan

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First published: 03 August 2004
Citations: 1
Nobuo Okabe, e-mail: [email protected]

Abstract

In the title compound, C8H8O4, the acetic acid side chain adopts a roughly perpendicular orientation with respect to the phenyl ring. Hydro­gen bonding between carboxyl groups results in the formation of a centrosymmetric dimer. An intramolecular hydrogen bond is formed in the catechol part of the mol­ecule. Molecules are linked together through hydrogen bonds between hydroxyl and carboxyl­ic acid O atoms.

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