n-Butylboronic acid MIDA ester

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Reagent Code: #148014
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CAS Number 1104637-43-5

science Other reagents with same CAS 1104637-43-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.039 g/mol
Formula C₉H₁₆BNO₄
badge Registry Numbers
MDL Number MFCD11215249
thermostat Physical Properties
Melting Point 122-128℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a stable and easily handled boron reagent. Its main advantage lies in its air and moisture stability, allowing for long-term storage and reliable performance in iterative synthesis. Commonly employed in automated and modular synthesis platforms, especially in pharmaceutical and agrochemical research where precise, stepwise construction of complex molecules is required. The MIDA protecting group enables controlled activation of the boronic acid, making it ideal for sequential coupling reactions without premature decomposition.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,420.00
inventory 5g
10-20 days ฿5,810.00
inventory 25g
10-20 days ฿14,030.00

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n-Butylboronic acid MIDA ester
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Used in Suzuki-Miyaura cross-coupling reactions as a stable and easily handled boron reagent. Its main advantage lies in its air and moisture stability, allowing for long-term storage and reliable performance in iterative synthesis. Commonly employed in automated and modular synthesis platforms, especially in pharmaceutical and agrochemical research where precise, stepwise construction of complex molecules is required. The MIDA protecting group enables controlled activation of the boronic acid, making it

Used in Suzuki-Miyaura cross-coupling reactions as a stable and easily handled boron reagent. Its main advantage lies in its air and moisture stability, allowing for long-term storage and reliable performance in iterative synthesis. Commonly employed in automated and modular synthesis platforms, especially in pharmaceutical and agrochemical research where precise, stepwise construction of complex molecules is required. The MIDA protecting group enables controlled activation of the boronic acid, making it ideal for sequential coupling reactions without premature decomposition.

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