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 |
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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 |
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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 |
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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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