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1-BROMO-2,4-DICHLOROBENZENE

Basic information Safety Supplier Related

1-BROMO-2,4-DICHLOROBENZENE Basic information

Product Name:
1-BROMO-2,4-DICHLOROBENZENE
Synonyms:
  • 1-BROMO-2,4-DICHLOROBENZENE
  • BROMO(2-)-4-DICHLOROBENZENE
  • 2,4-Dichloro Bromo Benzene 4'-Phenyl Acetophenone
  • 1-Bromo-2,4-dichlorobenzene, 98+%
  • 1-BROMO-2,4-DICHLOROBENZENE / 2,4-DICHLOROBROMOBENZENE
  • Benzene, 1-bromo-2,4-dichloro-
  • 2,4-DICHLOROBROMOBENZENE
  • 1-Bromo-2,4-dichlorobenzene,99%
CAS:
1193-72-2
MF:
C6H3BrCl2
MW:
225.9
EINECS:
214-778-6
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Benzene derivates
  • Bromine Compounds
  • Chlorine Compounds
  • Aryl
  • Halogenated Hydrocarbons
  • C6
Mol File:
1193-72-2.mol
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1-BROMO-2,4-DICHLOROBENZENE Chemical Properties

Melting point:
26-30 °C(lit.)
Boiling point:
235°C
Density 
1,89 g/cm3
refractive index 
1.5700 (estimate)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder to lump to clear liquid
color 
White or Colorless to Light yellow
Water Solubility 
Slightly soluble in water.
BRN 
1635733
InChI
InChI=1S/C6H3BrCl2/c7-5-2-1-4(8)3-6(5)9/h1-3H
InChIKey
ISHYFWKKWKXXPL-UHFFFAOYSA-N
SMILES
C1(Br)=CC=C(Cl)C=C1Cl
CAS DataBase Reference
1193-72-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
RIDADR 
UN 2810 6.1/PG 1
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29039990

MSDS

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1-BROMO-2,4-DICHLOROBENZENE Usage And Synthesis

Chemical Properties

colorless to light yellow crystalline mass or

Uses

1-Bromo-2,4-dichlorobenzene is used to produce 2,4,4'-trichloro-biphenyl. This reaction will need aq. Na2CO3 and solvents dioxane, ethanol. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.

General Description

1-Bromo-2,4-dichlorobenzene is an aryl halide. It can be distinguished from the other bromodichlorobenzene isomers using IR and Raman spectral data. It can undergo Suzuki–Miyaura cross-coupling reaction with arylboronic acids in the presence of different Suzuki catalysts.

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