4-Bromo-2-chlorotoluene

98%

Reagent Code: #144474
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Alias 2-Chloro-4-Bromotoluene
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CAS Number 89794-02-5

science Other reagents with same CAS 89794-02-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.48 g/mol
Formula C₇H₆BrCl
badge Registry Numbers
MDL Number MFCD00060651
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where selective halogen substitution is required, due to the differing reactivity of bromo and chloro groups. Commonly employed in cross-coupling reactions such as Suzuki or Ullmann reactions to construct carbon-carbon or carbon-heteroatom bonds. Also utilized in the development of specialty chemicals including dyes and functional materials where controlled substitution patterns are essential.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 98-100%
Appearance Colorless to light yellow liquid
Refractive Index (n20/D) 1.576-1.586
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿590.00
inventory 100g
10-20 days ฿2,090.00
inventory 500g
10-20 days ฿9,930.00
inventory 5g
10-20 days ฿310.00

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4-Bromo-2-chlorotoluene
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where selective halogen substitution is required, due to the differing reactivity of bromo and chloro groups. Commonly employed in cross-coupling reactions such as Suzuki or Ullmann reactions to construct carbon-carbon or carbon-heteroatom bonds. Also utilized in the development of specialty chemicals including dyes

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where selective halogen substitution is required, due to the differing reactivity of bromo and chloro groups. Commonly employed in cross-coupling reactions such as Suzuki or Ullmann reactions to construct carbon-carbon or carbon-heteroatom bonds. Also utilized in the development of specialty chemicals including dyes and functional materials where controlled substitution patterns are essential.

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