Chalcone

• Formula: C₁₅H₁₂O
• Molecular weight: 208.2552
• IUPAC Standard InChI: InChI=1S/C15H12O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-12H Copy

  
• IUPAC Standard InChIKey: DQFBYFPFKXHELB-UHFFFAOYSA-N Copy
• CAS Registry Number: 94-41-7
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • 2-Propen-1-one, 1,3-diphenyl-, (E)-
• Other names: 2-Propen-1-one, 1,3-diphenyl-; α-Benzylideneacetophenone; β-Benzoylstyrene; β-Phenylacrylophenone; Benzalacetophenone; Benzylideneacetophenone; Benzylidenacetophenone; Chalkone; Cinnamophenone; Phenyl styryl ketone; 1-Phenyl-2-benzoylethylene; 1,3-Diphenyl-1-propen-3-one; 2-Benzalacetophenone; 2-Benzylideneacetophenone; 3-Phenylacrylophenone; 1,3-Diphenyl-2-propen-1-one; Acrylophenone, 3-phenyl-; 1-Benzoyl-2-phenylethene; 1,3-Diphenylpropenone; Phenyl 2-phenylvinyl ketone; Styryl phenyl ketone; 1-Benzoyl-2-phenylethylene; ω-Benzylideneacetophenone; 1,3-Diphenyl-2-propenone; NSC 26612
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
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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 by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Gas Chromatography

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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

Van Den Dool and Kratz RI, non-polar column, temperature ramp

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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.

Kern, Shriner, et al., 1925
Kern, J.W.; Shriner, R.L.; Adams, R., Platinum and Palladium Oxides as Catalysts in the Reduction of Organic Compounds IX. The Reduction of Olefins, J. Am. Chem. Soc., 1925, 47, 1147. [all data]

Shapi and Hesso, 1990
Shapi, M.M.; Hesso, A., Thermal decomposition of polystyrene volatile compounds from large-scale pyrolysis, J. Anal. Appl. Pyrolysis, 1990, 18, 2, 143-161, https://doi.org/10.1016/0165-2370(90)80004-8 . [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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