2'-BROMO-4-CHLORO-BIPHENYL

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Products Intro: Product Name:2-bromo-2-(4-chlorophenyl)benzene
CAS:179526-95-5
Purity:99.5% Package:1KG;USD
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CAS:179526-95-5
Purity:>=99.0% Package:20kg;25kg Remarks:Hebei Maison Chemical has two production bases in Hebei and Ningxia,Its advantageous reactions include Grignard reaction, low-temperature butyl lithium reaction,SUZUKI reaction, an
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CAS:179526-95-5
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CAS:179526-95-5
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CAS:179526-95-5
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2'-BROMO-4-CHLORO-BIPHENYL manufacturers

  • 2-Bromo-4'-chloro-1,1'-biphenyl
  • 2-Bromo-4'-chloro-1,1'-biphenyl pictures
  • $200.00 / 1KG
  • 2025-09-25
  • CAS:179526-95-5
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • Supply Ability: g-kg-tons, free sample is available
2'-BROMO-4-CHLORO-BIPHENYL Basic information
Product Name:2'-BROMO-4-CHLORO-BIPHENYL
Synonyms:1,1'-Biphenyl, 2-bromo-4'-chloro-;2'-BROMO-4-CHLORO-BIPHENYL;2-Bromo-4'-chloro-1,1'-biphenyl;2-Bromo-4`-chloro-bipheny;1-bromo-2-(4-chlorophenyl)benzene;2-Bromo-4'-chloro-1'-biphenyl;2-bromo-2-(4-chlorophenyl)benzene;Boronic, B-(4'-chloro[1,1'-biphenyl]-2-yl)-
CAS:179526-95-5
MF:C12H8BrCl
MW:267.55
EINECS:
Product Categories:
Mol File:179526-95-5.mol
2'-BROMO-4-CHLORO-BIPHENYL Structure
2'-BROMO-4-CHLORO-BIPHENYL Chemical Properties
Melting point 41 °C
Boiling point 325.5±17.0 °C(Predicted)
density 1.463
storage temp. Sealed in dry,Room Temperature
form powder to lump
color White to Orange to Green
InChIInChI=1S/C12H8BrCl/c13-12-4-2-1-3-11(12)9-5-7-10(14)8-6-9/h1-8H
InChIKeyWSHZWUXRWQVZQP-UHFFFAOYSA-N
SMILESC1(C2=CC=C(Cl)C=C2)=CC=CC=C1Br
Safety Information
HS Code 2903.99.8001
MSDS Information
2'-BROMO-4-CHLORO-BIPHENYL Usage And Synthesis
Chemical Propertiesoff-white solid
Synthesis
1-Bromo-2-iodobenzene

583-55-1

4-Chlorophenylboronic acid

1679-18-1

2'-BROMO-4-CHLORO-BIPHENYL

179526-95-5

1-Bromo-2-iodobenzene (30 g, 106 mmol) and 4-chlorophenylboronic acid (16.9 g, 108.6 mmol) were added to an aqueous 2M potassium carbonate solution (100 ml) in dioxane solution. Subsequently, tetrakis(triphenylphosphine)palladium (2.45 g, 2 mol%) was added as a catalyst. The reaction mixture was heated and reacted under stirring for 4 hours. After completion of the reaction, it was cooled to room temperature and the reaction was quenched with potassium carbonate solution followed by separation of the aqueous and organic layers. After the organic layer was concentrated under reduced pressure to remove the solvent, it was purified by column chromatography (eluent: hexane) to afford the target product 2-bromo-4'-chloro-1,1'-biphenyl (A1) as a white solid (25.3 g, 90% yield).

References[1] Patent: KR2017/41159, 2017, A. Location in patent: Paragraph 0274-0276
[2] Organic Letters, 2015, vol. 17, # 2, p. 386 - 389
[3] Organic Letters, 2013, vol. 15, # 24, p. 6186 - 6189
[4] Advanced Synthesis and Catalysis, 2018, vol. 360, # 16, p. 3049 - 3054
[5] Chemical Communications, 2014, vol. 50, # 17, p. 2193 - 2195
2'-BROMO-4-CHLORO-BIPHENYL Preparation Products And Raw materials
Raw materials1-Bromo-2-iodobenzene-->4-Chlorophenylboronic acid-->1,2-Dibromobenzene-->Water-->Potassium carbonate-->Tetrakis(triphenylphosphine)palladium-->1,4-Dioxane
Preparation ProductsAZD4320
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