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3-Bromobenzenesulfonyl chloride

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3-Bromobenzenesulfonyl chloride Basic information

Product Name:
3-Bromobenzenesulfonyl chloride
Synonyms:
  • BUTTPARK 94\57-33
  • 3-BROMOBENZENE-1-SULFONYL CHLORIDE
  • 3-BROMOBENZENESULFONYL CHLORIDE
  • 3-BROMOBENZENESULPHONYL CHLORIDE
  • m-bromobenzenesulfonyl chloride
  • m-Bromobenzenesulfonyl
  • 3-Bromobenzenesulfonyl chloride,98%
  • Benzenesulfonyl chloride, 3-broMo-
CAS:
2905-24-0
MF:
C6H4BrClO2S
MW:
255.52
EINECS:
628-300-2
Product Categories:
  • Benzenesulfonyl chloride
  • Miscellaneous
  • Aryl
  • Organohalides
  • Sulfonyl Chloride
  • Organic Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds
  • alkyl bromide| alkyl chloride
Mol File:
2905-24-0.mol
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3-Bromobenzenesulfonyl chloride Chemical Properties

Melting point:
30-33 °C
Boiling point:
90-91 °C/0.5 mmHg (lit.)
Density 
1.773 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.593(lit.)
Flash point:
>110 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Liquid
color 
Clear colorless to yellow
Sensitive 
Moisture Sensitive
BRN 
2691656
Stability:
Moisture Sensitive
InChIKey
PJGOLCXVWIYXRQ-UHFFFAOYSA-N
CAS DataBase Reference
2905-24-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xn
Risk Statements 
34-36/37/38-20/21/22
Safety Statements 
26-36/37/39-45-36
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
Hazard Note 
Corrosive/Moisture Sensitive
HazardClass 
8
PackingGroup 
II
HS Code 
29049090

MSDS

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3-Bromobenzenesulfonyl chloride Usage And Synthesis

Chemical Properties

clear colorless to yellow liquid

Uses

3-Bromobenzenesulfonyl chloride may be used in the preparation of:

  • 2-(3-bromophenyl)-5-n-butylfuran
  • 2-(3-bromophenyl)-3,6-dimethyl-4,5,6,7-tetrahydrobenzofuran
  • 3-bromo-4-(3-bromophenyl)thiophene
  • 2,5-bis(3-bromophenyl)-1-methylpyrrole

General Description

3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.

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