ChemicalBook--->CAS DataBase List--->21554-71-2

21554-71-2

21554-71-2 Structure

21554-71-2 Structure
IdentificationBack Directory
[Name]

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-3-(4-hydroxyphenyl)-
[CAS]

21554-71-2
[Synonyms]

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-3-(4-hydroxyphenyl)-
[Molecular Formula]

C15H12O5
[MDL Number]

MFCD00276667
[MOL File]

21554-71-2.mol
[Molecular Weight]

272.25
Chemical PropertiesBack Directory
[Boiling point ]

577.9±50.0 °C(Predicted)
[density ]

1.485±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Ethyl Acetate (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

7.52±0.40(Predicted)
[color ]

Off-White to Pale Beige
[biological source]

synthetic
[Stability:]

Hygroscopic, Light sensitive
[InChI]

1S/C15H12O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-6,11,16-18H,7H2
[InChIKey]

UQGVUYNHDKMLSE-UHFFFAOYSA-N
[SMILES]

O1CC(C(=O)c3c1cc(cc3O)O)c2ccc(cc2)O
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
Hazard InformationBack Directory
[Uses]

Dihydrogenistein is a derivative of Genistein (G350000), a compound that exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor recepto r kinase.
[Uses]

Dihydrogenistein is a derivative of Genistein (G350000), a compound that exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase.
[Definition]

ChEBI: A hydroxyisoflavanone comprising isoflavanone carrying three hydroxy substituents at positions 5, 7 and 4'.
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