1,2-Dibromo-4,5-dimethylbenzene

98%(GC)

  • Product Code: 114035
  Alias:    4,5-Dibromo-O-xylene; 4,5-Dibromo-o-xylene
  CAS:    24932-48-7
Molecular Weight: 263.96 g./mol Molecular Formula: C₈H₈Br₂
EC Number: MDL Number: MFCD00082743
Melting Point: 85-89 °C(lit.) Boiling Point: 278 °C
Density: Storage Condition: room temperature
Product Description: 1,2-Dibromo-4,5-dimethylbenzene is primarily used in organic synthesis as a building block for more complex chemical compounds. Its bromine atoms make it highly reactive, allowing it to participate in various coupling reactions, such as Suzuki or Heck reactions, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a precursor in the synthesis of specialty chemicals, including dyes, pigments, and polymers, due to its ability to introduce specific functional groups into molecular structures. In research, it is often employed as a model compound to study electrophilic aromatic substitution reactions and bromination mechanisms. Its applications also extend to the development of flame retardants, where brominated aromatic compounds are valued for their thermal stability and effectiveness.
Product Specification:
Test Specification
Melting Point 85-89
Purity (GC) 98-100%
Appearance White To Off-white To Light Yellow To Light Red Powder, Crystals, Crystalline Powder Or Chunks
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $16.91
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5.000 10-20 days $42.27
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25.000 10-20 days $146.53
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100.000 10-20 days $556.52
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1,2-Dibromo-4,5-dimethylbenzene
1,2-Dibromo-4,5-dimethylbenzene is primarily used in organic synthesis as a building block for more complex chemical compounds. Its bromine atoms make it highly reactive, allowing it to participate in various coupling reactions, such as Suzuki or Heck reactions, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a precursor in the synthesis of specialty chemicals, including dyes, pigments, and polymers, due to its ability to introduce specific functional groups into molecular structures. In research, it is often employed as a model compound to study electrophilic aromatic substitution reactions and bromination mechanisms. Its applications also extend to the development of flame retardants, where brominated aromatic compounds are valued for their thermal stability and effectiveness.
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