(4-Pivalamidophenyl)boronic acid

96%

Reagent Code: #227537
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CAS Number 182344-22-5

science Other reagents with same CAS 182344-22-5

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scatter_plot Molecular Information
Weight 221.06 g/mol
Formula C₁₁H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD08235071
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in constructing biaryl scaffolds found in bioactive molecules. The pivalamido group enhances stability and influences electronic and steric properties, improving selectivity and yield in coupling reactions. Commonly employed in the synthesis of drug candidates and functional materials requiring precise molecular architecture.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,270.00
inventory 1g
10-20 days ฿11,500.00
inventory 5g
10-20 days ฿40,250.00

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(4-Pivalamidophenyl)boronic acid
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Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in constructing biaryl scaffolds found in bioactive molecules. The pivalamido group enhances stability and influences electronic and steric properties, improving selectivity and yield in coupling reactions. Commonly employed in the synthesi

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in constructing biaryl scaffolds found in bioactive molecules. The pivalamido group enhances stability and influences electronic and steric properties, improving selectivity and yield in coupling reactions. Commonly employed in the synthesis of drug candidates and functional materials requiring precise molecular architecture.

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