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2-Bromo-4-chloro-1-iodobenzene

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2-Bromo-4-chloro-1-iodobenzene manufacturers

2-Bromo-4-chloro-1-iodobenzene Basic information
Product Name:2-Bromo-4-chloro-1-iodobenzene
Synonyms:2-BROMO-4-CHLORO-1-IODOBENZENE;2-Bromo-1-iodo-4-chlorobenzene;1-Iodo-2-bromo-4-chlorobenzene;2-Bromo-4-chloro-1-iodobenzene >;Benzene, 2-bromo-4-chloro-1-iodo-
CAS:31928-44-6
MF:C6H3BrClI
MW:317.35
EINECS:608-682-7
Product Categories:Bromine Compounds;Chlorine Compounds;Iodine Compounds
Mol File:31928-44-6.mol
2-Bromo-4-chloro-1-iodobenzene Structure
2-Bromo-4-chloro-1-iodobenzene Chemical Properties
Melting point 32-35℃
Boiling point 279℃
density 2.272
Fp 123℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to lump to clear liquid
color White or Colorless to Yellow
Sensitive Light Sensitive
InChIInChI=1S/C6H3BrClI/c7-5-3-4(8)1-2-6(5)9/h1-3H
InChIKeyCXHXFDQEFKFYQJ-UHFFFAOYSA-N
SMILESC1(I)=CC=C(Cl)C=C1Br
CAS DataBase Reference31928-44-6
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37
Hazard Note Irritant
HS Code 29039990
MSDS Information
2-Bromo-4-chloro-1-iodobenzene Usage And Synthesis
Synthesis 2-Bromo-4-chloroaniline (10 g, 48 mmol) was suspended in hydrochloric acid water (50 mL of concentrated hydrochloric acid and 35 mL of water), and the suspension was cooled on a dry ice/methanol bath at -15°C. A sodium nitrite aqueous solution (3.6 g, 52 mmol, 1. 1 eq. /20 mL) was gradually added dropwise to it over 20 minutes, and the mixture was stirred from -15°C to 0°C for 30 minutes, thereby preparing a diazonium salt. The reaction solution was gradually added dropwise to a potassium iodide aqueous solution (73 g, 0.44 mol, 9 eq. /220 mL) at room temperature for 10 minutes. The reaction mixture was stirred at room temperature for 6 hours and then allowed to stand overnight. Dichloromethane (200 mL) was added to the reaction mixture, and subsequently, sodium hydrogensulfite (2 g) was added, deactivating the generated iodine. An organic layer was aliquoted, washed with a 10 % sodium hydrogensulfite aqueous solution (100 mL) and saturated salt water (30 mL) and dried over anhydrous magnesium sulfate. The solvent was then distilled off to obtain a red liquid. This was purified using column chromatography (silica gel/hexane) to obtain a white needle crystal 2-Bromo-4-chloro-1-iodobenzene (12.4 g, 81 %).
References[1] Patent: EP2316816, 2011, A1. Location in patent: Page/Page column 21
[2] Chemistry - A European Journal, 2018, vol. 24, # 55, p. 14622 - 14626
[3] Angewandte Chemie - International Edition, 2008, vol. 47, # 5, p. 888 - 890
[4] Angewandte Chemie - International Edition, 2008, vol. 47, # 9, p. 1726 - 1728
[5] Journal of Organic Chemistry, 1987, vol. 52, # 5, p. 748 - 753
2-Bromo-4-chloro-1-iodobenzene Preparation Products And Raw materials
Raw materials2-Bromo-4-chloroaniline-->Hydrochloric acid-->Sodium nitrite-->Potassium iodide
Preparation Products2-Chlorophenothiazine
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