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4-BROMO-1-CHLORO-2-IODOBENZENE

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Company Name: Hebei Xinsheng New Material Technology Co., LTD.
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Products Intro: Product Name:4-BROMO-1-CHLORO-2-IODOBENZENE
CAS:774608-49-0
Purity:99% Package:1kg;35USD|100kg;30USD|1000kg;25USD
Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name:4-BROMO-1-CHLORO-2-IODOBENZENE
CAS:774608-49-0
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Products Intro: Product Name:4-Bromo-1-chloro-2-iodobenzene
CAS:774608-49-0
Purity:98% Min. Package:1G;1KG;100KG
Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:4-bromo-1-chloro-2-iodobenzene
CAS:774608-49-0
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G
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Products Intro: Product Name:4-BROMO-1-CHLORO-2-IODOBENZENE
CAS:774608-49-0
Purity:99% Package:1KG;1USD

4-BROMO-1-CHLORO-2-IODOBENZENE manufacturers

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
EINECS:
Product Categories:Bromine Compounds;Chlorine Compounds;Iodine Compounds
Mol File:Mol File
4-BROMO-1-CHLORO-2-IODOBENZENE Structure
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
Safety Information
HS Code 2903998090
MSDS Information
4-BROMO-1-CHLORO-2-IODOBENZENE Usage And Synthesis
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
4-BROMO-1-CHLORO-2-IODOBENZENE Preparation Products And Raw materials
Raw materials4-BROMO-2-IODOANILINE-->Copper(II) chloride-->Acetonitrile-->tert-Butyl nitrite
Tag:4-BROMO-1-CHLORO-2-IODOBENZENE(774608-49-0) Related Product Information
1-Chloro-2-iodobenzene