1,3-Bis(trifluoromethyl)-5-bromobenzene

97%

  • Product Code: 71702
  Alias:    1,3-bis(trifluoromethyl)-5-bromobenzene; 3,5-bis(trifluoromethyl)bromobenzene
  CAS:    328-70-1
Molecular Weight: 293 g./mol Molecular Formula: C₈H₃BrF₆
EC Number: 206-334-5 MDL Number: MFCD00000381
Melting Point: −16 °C(lit.) Boiling Point: 154 °C(lit.)
Density: 1.699 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: Primarily utilized in organic synthesis, this compound serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical and agrochemical industries. Its trifluoromethyl groups enhance the stability and lipophilicity of the resulting compounds, making it valuable in the development of drugs with improved metabolic stability and membrane permeability. Additionally, it is employed in the synthesis of advanced materials, where its unique electronic properties contribute to the creation of organic semiconductors and liquid crystals. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the construction of diverse chemical structures.
Product Specification:
Test Specification
PurityGC 97-100
REFRACTIVE INDEX N20D 1.426-1.428
SPECIFIC GRAVITY 2020C 1.699-1.71
APPEARANCE COLORLESS LIQUID
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
2.000 10-20 days ฿300.00
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10.000 10-20 days ฿390.00
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50.000 10-20 days ฿750.00
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250.000 10-20 days ฿2,570.00
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1000.000 10-20 days ฿9,620.00
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1,3-Bis(trifluoromethyl)-5-bromobenzene
Primarily utilized in organic synthesis, this compound serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical and agrochemical industries. Its trifluoromethyl groups enhance the stability and lipophilicity of the resulting compounds, making it valuable in the development of drugs with improved metabolic stability and membrane permeability. Additionally, it is employed in the synthesis of advanced materials, where its unique electronic properties contribute to the creation of organic semiconductors and liquid crystals. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the construction of diverse chemical structures.
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