(4-Bromo-3,5-dimethylphenyl)boronic acid

98%

Reagent Code: #152838
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CAS Number 1451391-45-9

science Other reagents with same CAS 1451391-45-9

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its bromo and boronic acid functional groups allow dual reactivity, enabling sequential coupling steps in multi-component reactions. Commonly employed in the development of drug candidates and functional materials where controlled substitution patterns on aromatic rings are required. Stable under standard conditions and compatible with various catalysts, making it suitable for high-throughput synthesis and library generation in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿910.00

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(4-Bromo-3,5-dimethylphenyl)boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its bromo and boronic acid functional groups allow dual reactivity, enabling sequential coupling steps in multi-component reactions. Commonly employed in the development of drug candidates and functional materials where controlled substitution patterns on aromatic rings are required. Stable under standard conditions and compatible with various catalysts, makin

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its bromo and boronic acid functional groups allow dual reactivity, enabling sequential coupling steps in multi-component reactions. Commonly employed in the development of drug candidates and functional materials where controlled substitution patterns on aromatic rings are required. Stable under standard conditions and compatible with various catalysts, making it suitable for high-throughput synthesis and library generation in medicinal chemistry.

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