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DIPHENYLFULVENE

Basic information Physical form Uses Safety Supplier Related

DIPHENYLFULVENE Basic information

Product Name:
DIPHENYLFULVENE
Synonyms:
  • DIPHENYLFULVENE
  • 6,6-DIPHENYLFULVENE
  • 5-(DIPHENYLMETHYLENE)-1,3-CYCLOPENTADIENE
  • [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
CAS:
2175-90-8
MF:
C18H14
MW:
230.3
EINECS:
218-533-4
Product Categories:
  • Alkenes
  • Organic Building Blocks
  • Miscellaneous
  • Acyclic
Mol File:
2175-90-8.mol
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DIPHENYLFULVENE Chemical Properties

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)
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Safety Information

WGK Germany 
3
HS Code 
2902.90.9000

MSDS

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DIPHENYLFULVENE Usage And Synthesis

Physical form

Solid

Uses

6,6-Diphenylfulvene is a useful research chemical.

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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