Ethanone, 1-(3-hydroxyphenyl)-

• Formula: C₈H₈O₂
• Molecular weight: 136.1479
• IUPAC Standard InChI: InChI=1S/C8H8O2/c1-6(9)7-3-2-4-8(10)5-7/h2-5,10H,1H3 Copy

  
• IUPAC Standard InChIKey: LUJMEECXHPYQOF-UHFFFAOYSA-N Copy
• CAS Registry Number: 121-71-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Acetophenone, 3'-hydroxy-; m-Acetylphenol; m-Hydroxyacetophenone; 1-(3-Hydroxyphenyl)ethan-1-one; 3-Acetylphenol; 3'-Hydroxyacetophenone; 1-(3-Hydroxyphenyl)ethanone; 3-Hydroxyacetophenone; NSC 2440
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
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Normal melting point

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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: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

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.

Corey, Wright, et al., 1987
Corey, E.J.; Wright, S.W.; Mehrotra, M.M., Tetrahedron Lett., 1987, 28, 739-40. [all data]

Dannley and Hoffman, 1975
Dannley, R.L.; Hoffman, R.V., J. Org. Chem., 1975, 40, 2426-9. [all data]

Huckel and Thiele, 1961
Huckel, W.; Thiele, K., Chem. Ber., 1961, 94, 2027-31. [all data]

Iwata, Yoshikawa, et al., 1961
Iwata, E.; Yoshikawa, S.; Tsutsumi, S., Oxidation of Aromatic Compounds with Fenton Reagent, Kogyo Kagaku Zqasshi, 1961, 6, 463-6. [all data]

Renson and Huls, 1952
Renson, M.; Huls, R., Synthesis by Means of Organicadmium Derivatives. Preparation of Some m-Hydroxyacylophenones, Bull. Soc. Chim. Belges, 1952, 61, 599-608. [all data]

King, McWhirter, et al., 1945
King, L.C.; McWhirter, M.; Barton, D.M., Reactions of Acetophenols with Iodine and Pyridine and the Preparation of Hydroxybenzoic Acids, J. Am. Chem. Soc., 1945, 67, 2089-92. [all data]

Scaramelli, 1940
Scaramelli, G., Chelate-ring Formation XV. The Polarographic Reduction Potentials of Several Hydroxyacetophenones, Atti Accad. Italia, Rend. Classe Sci. Fis., 1940, 1940, 1 768-70. [all data]

Fuson, Lewis, et al., 1932
Fuson, R.C.; Lewis, P.H.; Du Puis, R.N., The Haloform Reaction V. The Influence of Ortho Bromo Atoms, J. Am. Chem. Soc., 1932, 54, 1114-20. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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