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 |
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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 |
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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 |
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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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