2-bromophenylboronic acid-1,3-propanediol ester

98%

Reagent Code: #148061
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CAS Number 959589-03-8

science Other reagents with same CAS 959589-03-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.90478 g/mol
Formula C₉H₁₂BBrO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester structure enhances stability and handling compared to the free boronic acid, improving reaction efficiency and selectivity. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules. Suitable for use in palladium-catalyzed transformations under mild conditions, making it valuable in medicinal chemistry and materials science.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿940.00
250mg
10-20 days ฿1,480.00
1g
10-20 days ฿3,680.00
5g
10-20 days ฿8,340.00
2-bromophenylboronic acid-1,3-propanediol ester
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Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester structure enhances stability and handling compared to the free boronic acid, improving reaction efficiency and selectivity. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules. Suitable for use in palladium-c

Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester structure enhances stability and handling compared to the free boronic acid, improving reaction efficiency and selectivity. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules. Suitable for use in palladium-catalyzed transformations under mild conditions, making it valuable in medicinal chemistry and materials science.

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