4-Bromo-2-chlorobenzotrifluoride

98%

  • Product Code: 119298
  Alias:    2-Chloro-4-bromobenzotrifluoride
  CAS:    467435-07-0
Molecular Weight: 259.45 g./mol Molecular Formula: C₇H₃BrClF₃
EC Number: MDL Number: MFCD08459292
Melting Point: Boiling Point:
Density: 1.76 Storage Condition: room temperature
Product Description: 4-Bromo-2-chlorobenzotrifluoride is widely used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure allows it to participate in coupling reactions, such as Suzuki or Sonogashira reactions, making it valuable for creating complex molecules. In pharmaceuticals, it serves as a building block for developing active ingredients, including potential drugs targeting specific biological pathways. In agrochemicals, it is utilized to produce herbicides, insecticides, and fungicides, contributing to crop protection and agricultural productivity. Additionally, its trifluoromethyl group enhances the stability and bioavailability of the final products, making it a preferred choice in chemical synthesis.
Product Specification:
Test Specification
Purity (GC) 98-100
Refractive Index N20/D 1.504-1.508
Specific Gravity (20/20) 1.757-1.761
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $29.10
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25.000 10-20 days $90.06
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4-Bromo-2-chlorobenzotrifluoride
4-Bromo-2-chlorobenzotrifluoride is widely used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure allows it to participate in coupling reactions, such as Suzuki or Sonogashira reactions, making it valuable for creating complex molecules. In pharmaceuticals, it serves as a building block for developing active ingredients, including potential drugs targeting specific biological pathways. In agrochemicals, it is utilized to produce herbicides, insecticides, and fungicides, contributing to crop protection and agricultural productivity. Additionally, its trifluoromethyl group enhances the stability and bioavailability of the final products, making it a preferred choice in chemical synthesis.
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