- Dihydrochalcone
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Dihydrochalcone 
1,3-diphenylpropan-1-oneOther namesHydrochalcone
Benzylacetophenone
Hydrocinnamophenone
3-Phenylpropiophenone
Phenethyl phenyl ketone
Phenyl phenethyl ketone
.beta.-Phenylpropiophenone
1,3-Diphenyl-1-propanone
.omega.-Benzyl acetophenoneIdentifiers PubChem 64802 ChemSpider 58334 
ChEMBL CHEMBL490512 Jmol-3D images Image 1 - C1=CC=C(C=C1)CCC(=O)C2=CC=CC=C2
- InChI=1S/C15H14O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-10H,11-12H2
Key: QGGZBXOADPVUPN-UHFFFAOYSA-N
Properties Molecular formula C15H14O Molar mass 210.27 g/mol Exact mass 210.104465 u Melting point 50 °C, 323 K, 122 °F
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Dihydrochalcone (DHC) is a chemical compound related to chalcone.
Dihydrochalcones (3′,5′-dihydroxy-2′,4′,6′-trimethoxydihydrochalcone, methyl linderone, 5-hydroxy-6,7,8-trimethoxyflavone (alnetin) and 2′-hydroxy-3′,4′,5′,6′-tetramethoxydihydrochalcone (dihydrokanakugiol) can be found in twigs of Lindera lucida.[1]
Known dihydrochacones
- Aspalathin, a C-linked dihydrochalcone glucoside found in rooibos, a common herbal tea
- Naringin dihydrochalcone, an artificial sweetener derived from naringin
- Neohesperidin dihydrochalcone, an artificial sweetener derived from citrus
- Nothofagin, a C-linked phloretin glucoside found in rooibos
- Phloretin
References
- ^ A dihydrochalcone from Lindera lucida. Yuan-Wah Leong, Leslie J. Harrison, , Graham J. Bennett, Azizol A. Kadir and Joseph D. Connolly, Phytochemistry, Volume 47, Issue 5, March 1998, Pp. 891-894, doi:10.1016/S0031-9422(97)00947-3
Dihydrochalcones: 3′,5′-dihydroxy-2′,4′,6′-trimethoxydihydrochalcone | 2′-hydroxy-3′,4′,5′,6′-tetramethoxydihydrochalcone (dihydrokanakugiol) | 2′-hydroxy-3′,4′,5′,6′-tetramethoxychalcone (kanakugiol) | 5-hydroxy-6,7,8-trimethoxyflavone (alnetin) | methyl linderone | 2′,3′,4′,5′,6′-pentamethoxychalcone (pedicellin) | Phloretin | Pinocembrin chalconeDihydrochalcone glycosides: 
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