4-BROMO-1-CHLORO-2-IODOBENZENE
4-BROMO-1-CHLORO-2-IODOBENZENE Basic information
- Product Name:
- 4-BROMO-1-CHLORO-2-IODOBENZENE
- Synonyms:
-
- 5-Bromo-2-chloroiodobenzene
- 4-BROMO-1-CHLORO-2-IODOBENZENE
- 1-Bromo-4-chloro-3-iodobenzene
- 2-Chloro-5-bromoiodobenzene
- 4-bromo-1-chloro-2-iodobenze
- Benzene, 4-bromo-1-chloro-2-iodo-
- 4-Bromo-1-Chloro-2-Iodobenzene 98%
- CAS:
- 774608-49-0
- MF:
- C6H3BrClI
- MW:
- 317.35
- Product Categories:
-
- Bromine Compounds
- Chlorine Compounds
- Iodine Compounds
- Mol File:
- Mol File
4-BROMO-1-CHLORO-2-IODOBENZENE Chemical Properties
- 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
4-BROMO-1-CHLORO-2-IODOBENZENE Usage And Synthesis
Synthesis
66416-72-6
7447-39-4
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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