Dihydrochalcone
Names | |
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IUPAC name
1,3-diphenylpropan-1-one | |
Other names
Hydrochalcone Benzylacetophenone Hydrocinnamophenone 3-Phenylpropiophenone Phenethyl phenyl ketone Phenyl phenethyl ketone .beta.-Phenylpropiophenone 1,3-Diphenyl-1-propanone .omega.-Benzyl acetophenone | |
Identifiers | |
3D model (Jmol) | Interactive image |
ChEMBL | ChEMBL490512 |
ChemSpider | 58334 |
ECHA InfoCard | 100.150.317 |
PubChem | 64802 |
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Properties | |
C15H14O | |
Molar mass | 210.27 g/mol |
Melting point | 50 °C (122 °F; 323 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Dihydrochalcone (DHC) is a chemical compound related to chalcone.
Dihydrochalcones (3′,5′-dihydroxy-2′,4′,6′-trimethoxydihydrochalcone, methyl linderone and 2′-hydroxy-3′,4′,5′,6′-tetramethoxydihydrochalcone (dihydrokanakugiol) can be found in twigs of Lindera lucida.[1]
Known dihydrochalcones
- 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
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