4-Bromo-2-chlorobenzotrifluoride
98%
Reagent
Code: #119298
Alias
2-Chloro-4-bromobenzotrifluoride
CAS Number
467435-07-0
blur_circular Chemical Specifications
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Molecular Information
Weight
259.45 g/mol
Formula
C₇H₃BrClF₃
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Registry Numbers
MDL Number
MFCD08459292
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Storage & Handling
Density
1.76
Storage
room temperature
description 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.
format_list_bulleted Product Specification
Test Parameter | 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 |
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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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