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2,4-Dimethylbromobenzene

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2,4-Dimethylbromobenzene Basic information

Product Name:
2,4-Dimethylbromobenzene
Synonyms:
  • 4-BROMO-M-XYLENE
  • 4-BROMO-1,3-DIMETHYLBENZENE
  • 1-Bromo-2,4-dimethyL
  • 2,4-DIMETHYLBROMOBENZENE
  • 1-BROMO-2,4-DIMETHYLBENZENE
  • 4-Bromo-1,3-dimethylbenzene~2,4-Dimethylbromobenzene
  • 4-BROMO-M-XYLENE 97%
  • 4-BROMO-M-XYLENE, TECH., 90%
CAS:
583-70-0
MF:
C8H9Br
MW:
185.06
EINECS:
209-517-8
Product Categories:
  • Aryl
  • Building Blocks
  • C8
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Halogen toluene
  • Benzene derivates
  • Bromine Compounds
  • Aromatic Hydrocarbons (substituted) & Derivatives
Mol File:
583-70-0.mol
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2,4-Dimethylbromobenzene Chemical Properties

Melting point:
-17°C
Boiling point:
214 °C(lit.)
Density 
1.37 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.551(lit.)
Flash point:
174 °F
storage temp. 
Sealed in dry,Room Temperature
Water Solubility 
Insoluble in water
form 
Liquid
color 
Clear colorless
CAS DataBase Reference
583-70-0(CAS DataBase Reference)
NIST Chemistry Reference
Benzene, 1-bromo-2,4-dimethyl-(583-70-0)
EPA Substance Registry System
4-Bromo-m-xylene (583-70-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29039990

MSDS

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2,4-Dimethylbromobenzene Usage And Synthesis

Chemical Properties

Clear colourless to light yellow liquid

Uses

4-Bromo-m-xylene is synthesized by the bromination of alkylbenzene substrates by N-bromosuccinimide.

General Description

Gold-catalyzed coupling reaction of pyrazine with 1-bromo-2,4-dimethylbenzene has been reported. 1-Bromo-2,4-dimethylbenzene reacts with Mg and DMF, followed by the reaction with I2 and aq.NH3 to afford the corresponding aromatic nitrile.

Synthesis

108-38-3

583-70-0

General procedure for the synthesis of 2,4-dimethylbromobenzene from m-xylene: N-bromosuccinimide (NBS, 1.0 mmol) and Catalyst 1 (gold loading of 0.1 or 1 mol% of the substrate) were accurately weighed and added to a 10 mL sealed reaction vessel, followed by 1,2-dichloroethane (DCE, 2 mL) and m-xylene (1.0 mmol). The reaction mixture was stirred at a set temperature for a specified time. After completion of the reaction, the catalyst was separated using a magnet and the reaction solution was concentrated under reduced pressure and purified by column chromatography.

References

[1] Russian Journal of Applied Chemistry, 2006, vol. 79, # 6, p. 949 - 956
[2] Canadian Journal of Chemistry, 2009, vol. 87, # 2, p. 440 - 447
[3] Tetrahedron Letters, 2013, vol. 54, # 9, p. 1063 - 1066
[4] Russian Journal of Organic Chemistry, 2005, vol. 41, # 11, p. 1631 - 1636
[5] Catalysis Letters, 2012, vol. 142, # 3, p. 378 - 383

2,4-Dimethylbromobenzene Preparation Products And Raw materials

Preparation Products

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