ChemicalBook--->CAS DataBase List--->2175-90-8

2175-90-8

2175-90-8 Structure

2175-90-8 Structure
IdentificationMore
[Name]

DIPHENYLFULVENE
[CAS]

2175-90-8
[Synonyms]

5-(DIPHENYLMETHYLENE)-1,3-CYCLOPENTADIENE
6,6'-DIPHENYLFULVENE
6,6-DIPHENYLFULVENE
DIPHENYLFULVENE
[2,4-Cyclopentadien-1-ylidene(phenyl)methyl]benzene
Diphenylmethylidene cyclopentadiene
Fulvene, 6,6-diphenyl
Methane, 2,4-cyclopentadien-1-ylidenediphenyl-
1,1'-[(2,4-Cyclopentadienylidene)methylene]bisbenzene
1-Diphenylmethylene-2,4-cyclopentadiene
5-(Diphenylmethylene)cyclopentadiene
5-Benzhydrylidene-1,3-cyclopentadiene
[EINECS(EC#)]

218-533-4
[Molecular Formula]

C18H14
[MDL Number]

MFCD00001419
[Molecular Weight]

230.3
[MOL File]

2175-90-8.mol
Questions And AnswerBack Directory
[Physical form]

Solid
[Uses]

6,6-Diphenylfulvene is a useful research chemical.
Chemical PropertiesBack Directory
[Melting point ]

81.5-83 °C (lit.)
[Boiling point ]

307.3°C (rough estimate)
[density ]

1.0829 (estimate)
[vapor pressure ]

0.033-0.084Pa at 25℃
[refractive index ]

1.5500 (estimate)
[storage temp. ]

Refrigerator
[form ]

Solid
[color ]

Light yellow to Brown
[InChI]

InChI=1S/C18H14/c1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16/h1-14H
[InChIKey]

BULLHRADHZGONG-UHFFFAOYSA-N
[SMILES]

C(/C1=CC=CC=C1)(\C1=CC=CC=C1)=C1\C=CC=C\1
[LogP]

3.43
[CAS DataBase Reference]

2175-90-8(CAS DataBase Reference)
[EPA Substance Registry System]

Benzene, 1,1'-(2,4-cyclopentadien-1-ylidenemethylene)bis- (2175-90-8)
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

2902.90.9000
Spectrum DetailBack Directory
[Spectrum Detail]

DIPHENYLFULVENE(2175-90-8)1HNMR
DIPHENYLFULVENE(2175-90-8)FT-IR
DIPHENYLFULVENE(2175-90-8)IR
DIPHENYLFULVENE(2175-90-8)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

2175-90-8(sigmaaldrich)
[TCI AMERICA]

6,6-Diphenylfulvene,>98.0%(GC)(2175-90-8)
Hazard InformationBack Directory
[Synthesis]

78.0 g (0.24 mol) of sodium methylate solution were initially introduced into a 500 ml four-necked flask at 50° C. and 45.6 g (0.25 mol) of benzophenone were then added. After complete dissolution, 20 g (0.30 mol) of freshly distilled cyclopentadiene were added dropwise in the course of 30 min at 45-50° C. After the end of the addition, stirring was effected for a further 2 h at room temperature, a dark red suspension forming. This was filtered over a G3 frit and the solid was washed four times with 25 ml of ethanol each time. After drying in a vacuum from an oil pump, 47.1 g (0.20 mol; 82% yield) of red 6,6-diphenylfulvene were obtained.
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