Identification | Back Directory | [Name]
1,5-DIPHENYL-1,5-PENTANEDIONE | [CAS]
6263-83-8 | [Synonyms]
TIMTEC-BB SBB008576 RARECHEM AQ A2 0032 1,3-DIBENZOYLPROPANE 1,3-Dibenzoylpropane 98% 1,5-diphenyl-5-pentanedione 1,5-DIPHENYL-1,5-PENTANEDIONE 1,5-DIPHENYLPENTANE-1,5-DIONE 1,5-Diphenyl-1,5-pentanedione,99% | [Molecular Formula]
C17H16O2 | [MDL Number]
MFCD00051401 | [MOL File]
6263-83-8.mol | [Molecular Weight]
252.31 |
Chemical Properties | Back Directory | [Appearance]
WHITE TO LIGHT BEIGE CRYSTALLINE POWDER | [Melting point ]
66-68 °C(lit.)
| [Boiling point ]
355.49°C (rough estimate) | [density ]
1.0832 (rough estimate) | [refractive index ]
1.5700 (estimate) | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [form ]
Crystalline Powder | [color ]
White to light beige | [EPA Substance Registry System]
1,5-Pentanedione, 1,5-diphenyl- (6263-83-8) |
Hazard Information | Back Directory | [Chemical Properties]
WHITE TO LIGHT BEIGE CRYSTALLINE POWDER | [Uses]
1,3-Dibenzoylpropane may be used in the electrochemical synthesis of cis-1,2-diphenyl-1,2-cyclopentanediol, via reduction in acetonitrile. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 38, p. 901, 1973 DOI: 10.1021/jo00945a011 Tetrahedron Letters, 15, p. 3721, 1974 | [General Description]
1,3-Dibenzoylpropane is a 1,3-diaroylpropane. 1,3-Dibenzoylpropane is formed during hydroxocobalt(III) Schiff base complexes catalyzed selective aldol reaction of dibenzoylmethanes with formaldehyde in methanol. |
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