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93413-00-4

93413-00-4 Structure

93413-00-4 Structure
IdentificationBack Directory
[Name]

(+)-3-[1-[Bis(4-hydroxyphenyl)methyl]-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one
[CAS]

93413-00-4
[Synonyms]

aechromone
Chamaechromone
(+)-Chamaechromone
3-[1,1-bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl]-5,7-dihydroxychromen-4-one
3-(1,1-Bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl)-5,7-dihydroxy-4H-chromen-4-one
(+)-3-'1-'Bis(4-hydroxyphenyl)methyl-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl-5,7-dihydroxy-4H-1-benzopyran-4-one
(+)-3-[1-[Bis(4-hydroxyphenyl)methyl]-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one
[Molecular Formula]

C30H22O10
[MDL Number]

MFCD27969124
[MOL File]

93413-00-4.mol
[Molecular Weight]

542.49
Chemical PropertiesBack Directory
[Boiling point ]

906.4±65.0 °C(Predicted)
[density ]

1.594±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

6.22±0.20(Predicted)
[color ]

Off-white to light yellow
Hazard InformationBack Directory
[Uses]

Chamaechromone is a biflavonoid ingredient isolated from the roots of Stellera chamaejasme L. (Thymelaeaceae). Chamaechromone possesses anti-hepatitis B virus (HBV) effects against the surface antigen of HBV (HBsAg) secretion and has insecticidal activities[1].
[References]

[1] Yan Lou, et al.Metabolites characterization of chamaechromone in vivo and in vitro by using ultra-performance liquid chromatography/Xevo G2 quadrupole time-of-flight tandem mass spectrometry. J Ethnopharmacol DOI:10.1016/j.jep.2013.10.027
Spectrum DetailBack Directory
[Spectrum Detail]

(+)-3-[1-[Bis(4-hydroxyphenyl)methyl]-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one(93413-00-4)1HNMR
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