ChemicalBook--->CAS DataBase List--->68745-38-0

68745-38-0

68745-38-0 Structure

68745-38-0 Structure
IdentificationBack Directory
[Name]

PINOCEMBRIN
[CAS]

68745-38-0
[Synonyms]

NSC 43318
PINOCEMBRIN
(±)-Pinocchio
DL-Pinocembrin
rac-PinoceMbrin
(+/-)-Pinocembrin
5,7-DIHYDROXYFLAVANONE
Pinocembrin racemate (DL0108)
5,7-DIHYDROXY-3'4'5'-FLAVANONE
5,7-Dihydroxy-2-phenyl-4-chromanone
5,7-DIHYDROXY-2-PHENYL-CHROMAN-4-ONE
5,7-Dihydroxyflavanone (Pinocembrin)
5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one
2-Phenyl-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one
5,7-Dihydroxy-2,3-dihydro-2-phenyl-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-
(2R)-5,7-dihydroxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one
[Molecular Formula]

C15H12O4
[MDL Number]

MFCD00017482
[MOL File]

68745-38-0.mol
[Molecular Weight]

256.25
Chemical PropertiesBack Directory
[Melting point ]

202-203°C
[Boiling point ]

511.1±50.0 °C(Predicted)
[density ]

1.386±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly, heated), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

7.50±0.40(Predicted)
[color ]

White to Pale Beige
[Major Application]

food and beverages
[InChI]

1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2/t13-/m0/s1
[InChIKey]

URFCJEUYXNAHFI-ZDUSSCGKSA-N
[SMILES]

OC1=CC(OC(C2=CC=CC=C2)C3)=C(C(O)=C1)C3=O
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Pinocembrin is a flavanoid with antioxidant activity found in damiana, honey, and propolis. Recent studies show that Pinocembrin maybe be a therapeutic option in reducing cerebral ischemia/reperfusion injury as a result of its anti-oxidative and anti-apoptotic effects. Pinocembrin displayed neuroprotective effects in glutamate injury model partly by inhibiting p53 expression causing a lower Bax-Bcl-2 ratio and by inhibiting the release of cytochrome c.
[Synthesis]

The synthesis of biopinein was carried out by the traditional chalcone closed-loop synthetic route, which requires chemical reagents that have the disadvantage of polluting the environment, reacting under drastic conditions, and consuming large amounts

Spectrum DetailBack Directory
[Spectrum Detail]

PINOCEMBRIN(68745-38-0)MS
PINOCEMBRIN(68745-38-0)1HNMR
PINOCEMBRIN(68745-38-0)IR1
PINOCEMBRIN(68745-38-0)IR2
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