Biphenyl-4-carboxylic acid

• Formula: C₁₃H₁₀O₂
• Molecular weight: 198.2173
• IUPAC Standard InChI: InChI=1S/C13H10O2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,(H,14,15) Copy

  
• IUPAC Standard InChIKey: NNJMFJSKMRYHSR-UHFFFAOYSA-N Copy
• CAS Registry Number: 92-92-2
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: 4-Biphenylcarboxylic acid; Biphenylcarboxylic acid-(4); [1,1'-Biphenyl]-4-carboxylic acid; p-Phenylbenzoic acid; Diphenyl-4-carboxylic acid; Para phenyl benzoic acid; 4-Carboxy-1,1'-biphenyl; 4-Carboxybiphenyl; 4-Diphenylcarboxylic acid; 4-Phenylbenzoic acid; NSC 23040; Benzoic acid, p-phenyl-
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • References
  • Notes
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  • X-ray Photoelectron Spectroscopy Database, version 5.0
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Coblentz Society, Inc.

Spectrum

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Additional Data

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Hammond and Todd, 1954
Hammond, G.S.; Todd, R.W., The Low Reactivity of Cyclopropane Derivatives twoard Free Radicals, J. Am. Chem. Soc., 1954, 76, 4081. [all data]

Matos, Miranda, et al., 2004
Matos, M. Agostinha R.; Miranda, Margarida S.; Martins, Diana V.S.S.; Pinto, Nat«65533»lia A.B.; Morais, Victor M.F.; Liebman, Joel F., Thermochemistry of biphenylcarboxylic and dicarboxylic acids. A combined experimental and theoretical studyThis paper is dedicated to Kurt Mislow, a pioneering biphenyl stereochemist, on the occasion of his 80th birthday., Org. Biomol. Chem., 2004, 2, 9, 1353, https://doi.org/10.1039/b401605j . [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔsubH°	Enthalpy of sublimation at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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