n-Butylboronic acid pinacol ester

98%

Reagent Code: #91159
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CAS Number 69190-62-1

science Other reagents with same CAS 69190-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.08 g/mol
Formula C₁₀H₂₁BO₂
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MDL Number MFCD03789255
inventory_2 Storage & Handling
Density 0.865 g/mL
Storage Room temperature, dry, inert gas storage

description Product Description

n-Butylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The compound acts as a stable and efficient boron reagent, enabling the coupling of aryl or vinyl halides with organoboron compounds. Its pinacol ester group enhances stability, making it easier to handle and store compared to other boronic acid derivatives. Additionally, it is employed in the preparation of complex molecules, including natural products and polymers, due to its compatibility with various functional groups and reaction conditions.

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Test Parameter Specification
Appearance Liquid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿240.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿1,580.00

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n-Butylboronic acid pinacol ester
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n-Butylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The compound acts as a stable and efficient boron reagent, enabling the coupling of aryl or vinyl halides with organoboron compounds. Its pinacol ester group enhances stability, making it easier to handle and store compared to

n-Butylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The compound acts as a stable and efficient boron reagent, enabling the coupling of aryl or vinyl halides with organoboron compounds. Its pinacol ester group enhances stability, making it easier to handle and store compared to other boronic acid derivatives. Additionally, it is employed in the preparation of complex molecules, including natural products and polymers, due to its compatibility with various functional groups and reaction conditions.

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