ChemicalBook--->CAS DataBase List--->35225-79-7

35225-79-7

35225-79-7 Structure

35225-79-7 Structure
IdentificationMore
[Name]

DIBENZYLIDENEACETONE
[CAS]

35225-79-7
[Synonyms]

1,5-DIPHENYL-1,4-PENTADIEN-3-ONE
1,5-DIPHENYL-3-PENTADIENONE
1,5-DIPHENYL-PENTA-1,4-DIEN-3-ONE
AKOS 213-33
DBA
DIBENZAL ACETONE
DIBENZYLIDENEACETONE
DISTYRYL KETONE
TRANS,TRANS-1,5-DIPHENYL-1,4-PENTADIEN-3-ONE
TRANS,TRANS-1,5-DIPHENYLPENTA-1,4-DIEN-3-ONE
TRANS,TRANS-DIBENZALACETONE
TRANS,TRANS-DIBENZYLIDENEACETONE
TRANS,TRANS-DISTYRYL KETONE
trans,trans-Dibenzylideneacetone, 98+%
1,5-Diphenyl-1,4-pentadien-3-one, trans,trans-1,5-Diphenyl-1,4-pentadien-3-one
[EINECS(EC#)]

208-697-5
[Molecular Formula]

C17H14O
[MDL Number]

MFCD00004790
[Molecular Weight]

234.29
[MOL File]

35225-79-7.mol
Chemical PropertiesBack Directory
[Appearance]

yellow shiny crystalline powder
[Melting point ]

104-107 °C (lit.)
[Boiling point ]

336.62°C (rough estimate)
[density ]

1.0477 (rough estimate)
[refractive index ]

1.5000 (estimate)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

acetone: soluble(lit.)
[form ]

Crystalline Powder
[color ]

Yellow
[Water Solubility ]

Soluble in chloroform, acetone, alcohol (slightly), and hot methanol. Insoluble in water.
[Detection Methods]

HPLC
[Merck ]

14,3006
[BRN ]

608434
[InChIKey]

WMKGGPCROCCUDY-PHEQNACWSA-N
[CAS DataBase Reference]

35225-79-7(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

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

3
[HS Code ]

29143990
Hazard InformationBack Directory
[Chemical Properties]

Yellow crystalline powder
[Uses]

Reactant involved in:• ;Nazarov-like cyclization1• ;Transfer hydrogenation2• ;Lewis acid mediated condensation3• ;Hetero-Diels-Alder reactions4• ;Asymmetric 1,4-addition reactions5• ;Michael addition reactions6
[Uses]

trans,trans-Dibenzylideneacetone was used as an additive in the copper-catalyzed-arylation of imidazoles. It is a reactant involved in Nazarov-like cyclization, Transfer hydrogenation, Lewis acid mediated condensation, Hetero-Diels-Alder reactions, Asymmetric 1,4-addition reactions and Michael addition reactions.
[Application]

Reactant involved in:
Nazarov-like cyclization
Transfer hydrogenation
Lewis acid mediated condensation
Hetero-Diels-Alder reactions
Asymmetric 1,4-addition reactions
Michael addition reactions
trans,trans-Dibenzylideneacetone was used as an additive in the copper-catalyzed N-arylation of imidazoles.
Spectrum DetailBack Directory
[Spectrum Detail]

trans,trans-Dibenzylideneacetone(35225-79-7)1HNMR
trans,trans-Dibenzylideneacetone(35225-79-7)FT-IR
trans,trans-Dibenzylideneacetone(35225-79-7)Raman
trans,trans-Dibenzylideneacetone(35225-79-7)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

trans,trans-Dibenzylideneacetone, 96%(35225-79-7)
[Alfa Aesar]

trans,trans-Dibenzylideneacetone, 98+%(35225-79-7)
[Sigma Aldrich]

35225-79-7(sigmaaldrich)
[TCI AMERICA]

trans,trans-1,5-Diphenyl-1,4-pentadien-3-one,>99.0%(GC)(35225-79-7)
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