1-Bromo-4-(tert-butyl)-2-chlorobenzene

96%

Reagent Code: #146109
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CAS Number 1251032-65-1

science Other reagents with same CAS 1251032-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.56 g/mol
Formula C₁₀H₁₂BrCl
inventory_2 Storage & Handling
Storage Room temperature, dry

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 substitution is required due to the presence of both bromo and chloro functional groups. Its tert-butyl group provides steric bulk, influencing reaction selectivity in metal-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the development of liquid crystals and specialty polymers where halogenated aromatic structures enhance material stability and electronic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿940.00
inventory 5g
10-20 days ฿3,720.00
inventory 25g
10-20 days ฿17,970.00

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1-Bromo-4-(tert-butyl)-2-chlorobenzene
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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 substitution is required due to the presence of both bromo and chloro functional groups. Its tert-butyl group provides steric bulk, influencing reaction selectivity in metal-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the development of liquid crystals and specialty polyme

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 substitution is required due to the presence of both bromo and chloro functional groups. Its tert-butyl group provides steric bulk, influencing reaction selectivity in metal-coupling reactions such as Suzuki or Ullmann couplings. Also employed in the development of liquid crystals and specialty polymers where halogenated aromatic structures enhance material stability and electronic properties.

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