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3480-11-3

3480-11-3 Structure

3480-11-3 Structure
IdentificationBack Directory
[Name]

5-BROMO-2 2'-BITHIOPHENE 96
[CAS]

3480-11-3
[Synonyms]

2T-Br
5-Bromo-alpha-dithienyl
5-Bromo-[2,2']bithiophenyl
2,2'-Bithiophene, 5-bromo-
5-BROMO-2 2'-BITHIOPHENE 96
5-BroMo-2,2'-bithiophene 96%
2,2'-Bithiophene, 5-bromo-
5-Bromo-2,2'-bithiophene USP/EP/BP
[Molecular Formula]

C8H5BrS2
[MDL Number]

MFCD01461947
[MOL File]

3480-11-3.mol
[Molecular Weight]

245.16
Chemical PropertiesBack Directory
[Melting point ]

29-32 °C(lit.)
[Boiling point ]

50 °C(Press: 0.006 Torr)
[density ]

1.635±0.06 g/cm3(Predicted)
[Fp ]

>230 °F
[storage temp. ]

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

OMOAIGVIYUXYAU-UHFFFAOYSA-N
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Danger
[Hazard statements ]

H317-H334
[Precautionary statements ]

P501-P261-P272-P280-P284-P302+P352-P342+P311-P362+P364-P304+P340-P333+P313
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

5-Bromo-2,2′-bithiophene may be used in the synthesis of trimethyl-[2,2′;5′,2″;5″,2″]quaterthiophen-5-yl-silane (4TTMS) and 5-hexylsulfanyl-2,2′:5′,2′′-terthiophene.
[General Description]

5-Bromo-2,2′-bithiophene is a bromothiophene derivative. Its reaction with various aryl iodides bearing an electron-donating or electron-withdrawing substituent has been described. It can be synthesized from 2,2′-bithiophene.
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