Phenylboronic acid pinacol ester

98%

Reagent Code: #91219
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Alias 2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborinane
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CAS Number 24388-23-6

science Other reagents with same CAS 24388-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.07 g/mol
Formula C₁₂H₁₇BO₂
badge Registry Numbers
MDL Number MFCD00966985
thermostat Physical Properties
Melting Point 27-31 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Phenylboronic 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 production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a stable and easily handled precursor to phenylboronic acid, which is reactive in these coupling processes. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its compatibility with various functional groups. Its stability under normal conditions makes it a preferred choice in laboratory and industrial settings for efficient and selective chemical transformations.

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Test Parameter Specification
Purity (GC) 98-100%
Melting Point 27-31
Appearance White to yellow solid or liquid
Infrared Spectrum Conforms to Structure
Note This product is a low melting point solid and may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿410.00
inventory 25g
10-20 days ฿1,360.00
inventory 100g
10-20 days ฿4,290.00

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Phenylboronic acid pinacol ester
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Phenylboronic 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 production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a stable and easily handled precursor to phenylboronic acid, which is reactive in these coupling processes. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its compatibility with various functional groups. Its stability under normal conditions makes it a preferred choice in laboratory and industrial settings for efficient and selective chemical transformations.
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