ChemicalBook--->CAS DataBase List--->1607-57-4

1607-57-4

1607-57-4 Structure

1607-57-4 Structure
IdentificationMore
[Name]

Bromotriphenylethylene
[CAS]

1607-57-4
[Synonyms]

1-bromo-1,2,2-triphenylethylene
2-BROMO-1,1,2-TRIPHENYLETHYLENE
AURORA KA-6594
BROMOTRIPHENYLETHYLENE
alpha’-bromo-alpha-phenyl-stilben
bromotriphenyl-ethylen
Benzene, 1,1,1-(1-bromo-1-ethenyl-2-ylidene)tris-
à-bromo-à'-phenylstilbene
triphenylvinyl bromide
phenylstilbene bromide
Bromotriphenylethylene, 98+%
[2-Bromo-1,2-di(phenyl)ethenyl]benzene
alpha'-bromo-alpha-phenylstilbene
Bromotriphenylethene
1,1',1''-(1-Bromoethene-1,2,2-triyl)trisbenzene
1,1,2-Triphenyl-2-bromoethene
1-Bromo-1,2,2-triphenylethene
2-Bromo-1,1,2-triphenylethene
Eitriphin
α,β-Diphenylstyryl bromide
[EINECS(EC#)]

216-531-8
[Molecular Formula]

C20H15Br
[MDL Number]

MFCD00000135
[Molecular Weight]

335.24
[MOL File]

1607-57-4.mol
Chemical PropertiesBack Directory
[Appearance]

light yellow crystalline powder
[Melting point ]

115-117 °C(lit.)
[Boiling point ]

391.41°C (rough estimate)
[density ]

1.3419 (rough estimate)
[refractive index ]

1.6000 (estimate)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder to crystal
[color ]

Light orange to Yellow to Green
[BRN ]

2052962
[CAS DataBase Reference]

1607-57-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)
GHS08
[Signal word ]

Warning
[Hazard statements ]

H361
[Precautionary statements ]

P201-P202-P280-P308+P313-P405-P501a
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[RTECS ]

KU8850000
[HS Code ]

29036990
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

1-Bromo-1,2,2-triphenylethylene(1607-57-4).msds
Hazard InformationBack Directory
[Chemical Properties]

light yellow crystalline powder
[Synthesis]

Triphenylethylene

58-72-0

Bromotriphenylethylene

1607-57-4

GENERAL METHOD: Tristyrene (1.0 g, 3.49 mmol) was dissolved in chloroform (15 mL) and a chloroform (10 mL) solution of bromine (0.49 g, 3.06 mmol) was added slowly and dropwise. Upon completion of the reaction, the reaction mixture was decanted and the solvent was subsequently removed by distillation. The residue was recrystallized twice from ethanol to give triphenylene bromide (0.8 g, 62%) as colorless needle-like crystals.

[References]

[1] Bulletin of the Chemical Society of Japan, 1988, vol. 61, p. 449 - 454
[2] Chemische Berichte, 1987, vol. 120, p. 1897 - 1904
[3] Tetrahedron, 2012, vol. 68, # 36, p. 7309 - 7316
[4] Journal of the Chemical Society, 1933, p. 69,74
[5] Journal of the American Chemical Society, 1932, vol. 54, p. 2049,2051
Spectrum DetailBack Directory
[Spectrum Detail]

Bromotriphenylethylene(1607-57-4)MS
Bromotriphenylethylene(1607-57-4)IR1
Bromotriphenylethylene(1607-57-4)IR2
Bromotriphenylethylene(1607-57-4)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Bromotriphenylethylene, 98%(1607-57-4)
[Alfa Aesar]

Bromotriphenylethylene, 98+%(1607-57-4)
[TCI AMERICA]

2-Bromo-1,1,2-triphenylethylene,>98.0%(GC)(1607-57-4)
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