ChemicalBook--->CAS DataBase List--->495-71-6

495-71-6

495-71-6 Structure

495-71-6 Structure
IdentificationMore
[Name]

1,2-DIBENZOYLETHANE
[CAS]

495-71-6
[Synonyms]

1,2-DIBENZOYLETHANE
1,4-DIPHENYL-1,4-BUTANEDIONE
1,4-DIPHENYL-BUTANE-1,4-DIONE
DIBENZOYL ETHANE
TIMTEC-BB SBB008126
1,4-diphenyl-1,4-butadione
2,2’’-biacetophenone
2,2''-Biacetophenone
Biphenacyl
Ethane, 1,2-dibenzoyl-
1 4-DIPHENYL-1 4-BUTANEDIONE 95%
1,2-DIBENZOYLETHANE 98+%
1 2-DIBENZOYLETHANE 95%
β-Benzoylpropiophenone
[Molecular Formula]

C16H14O2
[MDL Number]

MFCD00037818
[Molecular Weight]

238.28
[MOL File]

495-71-6.mol
Chemical PropertiesBack Directory
[Melting point ]

144-145°C
[Boiling point ]

260 °C / 15mmHg
[density ]

1.116±0.06 g/cm3(Predicted)
[storage temp. ]

Refrigerator
[solubility ]

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

Solid
[color ]

White to Off-White
[Water Solubility ]

Soluble in acetone. Insoluble in water.
[BRN ]

782937
[CAS DataBase Reference]

495-71-6(CAS DataBase Reference)
[NIST Chemistry Reference]

1,4-Butanedione, 1,4-diphenyl-(495-71-6)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[HS Code ]

2914.39.9000
Hazard InformationBack Directory
[Uses]

1,2-Dibenzoylethane is effective in inhibiting the in vivo mammary DMBA-DNA adduct formation. This inhibitory effect on mammary DNA adduct formation was associated with increased liver activities of glutathione S-transferase, QR, and 7-ethoxyresorufin-O-deethylase.
[Uses]

It is effective in inhibiting the in vivo mammary DMBA-DNA adduct formation. This inhibitory effect on mammary DNA adduct formation was associated with increased liver activities of glutathione S-transferase, QR, and 7-ethoxyresorufin-O-deethylase.
[Synthesis Reference(s)]

Chemical and Pharmaceutical Bulletin, 28, p. 262, 1980 DOI: 10.1248/cpb.28.262
Journal of the American Chemical Society, 91, p. 687, 1969 DOI: 10.1021/ja01031a029
Tetrahedron Letters, 29, p. 3717, 1988 DOI: 10.1016/S0040-4039(00)82162-0
[Synthesis]

1,2-Dibenzoylethane can be prepared in a single step from racemic allyl secondary alcohol (±).

Spectrum DetailBack Directory
[Spectrum Detail]

1,2-DIBENZOYLETHANE(495-71-6)MS
1,2-DIBENZOYLETHANE(495-71-6)IR1
1,2-DIBENZOYLETHANE(495-71-6)IR2
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

1,2-Dibenzoylethane, 98+%(495-71-6)
[Sigma Aldrich]

495-71-6(sigmaaldrich)
[TCI AMERICA]

1,4-Diphenyl-1,4-butanedione,>98.0%(GC)(495-71-6)
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