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774608-49-0

774608-49-0 Structure

774608-49-0 Structure
IdentificationBack Directory
[Name]

4-BROMO-1-CHLORO-2-IODOBENZENE
[CAS]

774608-49-0
[Synonyms]

5-Bromo-2-chloroiodobenzene
2-Chloro-5-bromoiodobenzene
4-bromo-1-chloro-2-iodobenze
4-BROMO-1-CHLORO-2-IODOBENZENE
1-Bromo-4-chloro-3-iodobenzene
Benzene, 4-bromo-1-chloro-2-iodo-
[Molecular Formula]

C6H3BrClI
[MDL Number]

MFCD07780669
[MOL File]

774608-49-0.mol
[Molecular Weight]

317.35
Chemical PropertiesBack Directory
[Boiling point ]

283.3±25.0 °C(Predicted)
[density ]

2.272±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[form ]

liquid
[color ]

Clear, yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMO-1-CHLORO-2-IODOBENZENE(774608-49-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-BROMO-2-IODOANILINE

66416-72-6

Copper(II) chloride

7447-39-4

4-BROMO-1-CHLORO-2-IODOBENZENE

774608-49-0

Example 187: Synthesis of 6-(5-bromo-2-chloro-phenyl)-N*4*-(4-chloro-phenyl)-pyrimidine-2,4-diamine. To a stirred solution of copper(II) chloride suspension (1.62 g, 12.0 mmol) and tert-butyl nitrite (15.0 mmol) in acetonitrile (40 ml) was heated to 60°C. Subsequently, an acetonitrile solution (10 ml) of 4-bromo-2-iodoaniline (2.98 g, 10.0 mmol) was added dropwise over 50 min. The reaction mixture was continued to be stirred at 60 °C for 1 hour. After completion of the reaction, the mixture was poured into 20% hydrochloric acid (200 ml) and extracted with ether (2 x 30 ml). The crude product was purified by rapid chromatography on silica gel using hexane as eluent to give 4-bromo-1-chloro-2-iodobenzene (2.4 g, 76% yield).

[References]

[1] Patent: US2004/204386, 2004, A1
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