2-Hydroxybiphenyl-3-carboxylic acid (3-phenylsalicylic acid)

Allison J. Amonette; Roger E. Gerkin

doi:10.1107/S0108270196010530

2-Hydroxybiphenyl-3-carboxylic acid (3-phenylsalicylic acid)

Allison J. Amonette
, Roger E. Gerkin

Biochemistry, Chemistry & Physics

Ohio State University

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

In the title compound, C 13 H 10 O 3 , there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid.

Original language	English
Pages (from-to)	3088-3091
Number of pages	4
Journal	Acta Crystallographica Section C: Crystal Structure Communications
Volume	52
Issue number	12
DOIs	https://doi.org/10.1107/S0108270196010530
State	Published - Dec 15 1996

Scopus Subject Areas

General Biochemistry, Genetics and Molecular Biology

Access to Document

10.1107/S0108270196010530License: Unspecified

Cite this

@article{1a6c9e392f4a41e686ee187342350434,

title = "2-Hydroxybiphenyl-3-carboxylic acid (3-phenylsalicylic acid)",

abstract = " In the title compound, C 13 H 10 O 3 , there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid. ",

author = "Amonette, \{Allison J.\} and Gerkin, \{Roger E.\}",

note = "In the title compound, CHO, there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid.",

year = "1996",

month = dec,

day = "15",

doi = "10.1107/S0108270196010530",

language = "English",

volume = "52",

pages = "3088--3091",

journal = "Acta Crystallographica Section C: Crystal Structure Communications",

issn = "0108-2701",

publisher = "International Union of Crystallography",

number = "12",

}

TY - JOUR

T1 - 2-Hydroxybiphenyl-3-carboxylic acid (3-phenylsalicylic acid)

AU - Amonette, Allison J.

AU - Gerkin, Roger E.

N1 - In the title compound, CHO, there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid.

PY - 1996/12/15

Y1 - 1996/12/15

N2 - In the title compound, C 13 H 10 O 3 , there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid.

AB - In the title compound, C 13 H 10 O 3 , there is a single type of intermolecular hydrogen bond. From this is formed a cyclic dimer about a twofold axis. In addition, there is an intramolecular hydrogen bond which is virtually identical to that observed in salicylic acid.

UR - https://www.scopus.com/pages/publications/0030382981

U2 - 10.1107/S0108270196010530

DO - 10.1107/S0108270196010530

M3 - Article

SN - 0108-2701

VL - 52

SP - 3088

EP - 3091

JO - Acta Crystallographica Section C: Crystal Structure Communications

JF - Acta Crystallographica Section C: Crystal Structure Communications

IS - 12

ER -

2-Hydroxybiphenyl-3-carboxylic acid (3-phenylsalicylic acid)

Abstract

Scopus Subject Areas

Access to Document

Other files and links

Fingerprint

Cite this