4-Bromo-1-butylboronic acid catechol ester

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Reagent Code: #149474
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CAS Number 142172-51-8

science Other reagents with same CAS 142172-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.92 g/mol
Formula CH₁₂BBrO₂
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MDL Number MFCD01863716
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronic ester functionality provides enhanced stability and handling compared to the corresponding boronic acid. The 4-bromo substituent allows for further functionalization or coupling, making it a valuable building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Commonly employed in the development of conjugated systems such as biaryls and extended π-frameworks found in materials science and medicinal chemistry.

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inventory 1g
10-20 days ฿20,470.00

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4-Bromo-1-butylboronic acid catechol ester
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Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronic ester functionality provides enhanced stability and handling compared to the corresponding boronic acid. The 4-bromo substituent allows for further functionalization or coupling, making it a valuable building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Commonly employed in the development o

Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronic ester functionality provides enhanced stability and handling compared to the corresponding boronic acid. The 4-bromo substituent allows for further functionalization or coupling, making it a valuable building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Commonly employed in the development of conjugated systems such as biaryls and extended π-frameworks found in materials science and medicinal chemistry.

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