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16198-01-9

16198-01-9 Structure

16198-01-9 Structure
IdentificationBack Directory
[Name]

(+)-Catechin-pentaacetate
[CAS]

16198-01-9
[Synonyms]

Catechol pentaacetate
(+)-Catechin-pentaacetate
2α-[3,4-Bis(acetyloxy)phenyl]chroman-3β,5,7-triol 3,5,7-triacetate
3,4-Dihydro-2α-(3,4-diacetoxyphenyl)-3β,5,7-triacetoxy-2H-1-benzopyran
(2R)-2α-(3,4-Diacetoxyphenyl)-3β,5,7-triacetoxy-3,4-dihydro-2H-1-benzopyran
(2R)-3,4-Dihydro-2α-(3,4-dihydroxyphenyl)-2H-1-benzopyran-3β,5,7-triol pentaacetate
2H-1-Benzopyran-3,5,7-triol,2-[3,4-bis(acetyloxy)phenyl]-3,4-dihydro-, 3,5,7-triacetate, (2R,3S)-
[Molecular Formula]

C25H24O11
[MOL File]

16198-01-9.mol
[Molecular Weight]

500.45
Chemical PropertiesBack Directory
[Melting point ]

130-132 °C
[Boiling point ]

624.2±55.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Powder
Hazard InformationBack Directory
[Uses]

(+)-Catechin pentaacetate is a precursor for the production of (+) catechin (HY-N0898 ). (+) catechin is a useful natural herbicide and antimicrobial. (+)-Catechin inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM[1][2].
[target]

Antifection
[References]

[1] Veluri R, et al. Phytotoxic and antimicrobial activities of catechin derivatives. J Agric Food Chem. 2004 Mar 10;52(5):1077-82. DOI:10.1021/jf030653+
[2] Waffo-Téguo P, et al. Potential cancer-chemopreventive activities of wine stilbenoids and flavans extracted from grape (Vitis vinifera) cell cultures. Nutr Cancer. 2001;40(2):173-9. DOI:10.1207/S15327914NC402_14
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