Benzylboronic acid pinacol ester

97%

Reagent Code: #91202
label
Alias 2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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CAS Number 87100-28-5

science Other reagents with same CAS 87100-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.1 g/mol
Formula C₁₃H₁₉BO₂
badge Registry Numbers
MDL Number MFCD05663841
thermostat Physical Properties
Boiling Point 65 °C0.15 mm Hg
inventory_2 Storage & Handling
Density 0.980 g/mL at 25 °C
Storage room temperature

description Product Description

Benzylboronic 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, enabling the construction of complex molecules in pharmaceuticals, agrochemicals, and materials science. The compound serves as a stable and reactive boronic ester, facilitating the introduction of benzyl groups into target molecules. Its stability under various conditions makes it a preferred reagent in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds and functional materials due to its efficient reactivity and compatibility with diverse reaction conditions.

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Test Parameter Specification
Purity (GC) 97-100
Refractive Index (N20D) 1.486-1.49
Specific Gravity (20°C) 0.983-0.987
Appearance Colorless to pale yellow liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,080.00
inventory 25g
10-20 days ฿4,260.00

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Benzylboronic acid pinacol ester
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Benzylboronic 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, enabling the construction of complex molecules in pharmaceuticals, agrochemicals, and materials science. The compound serves as a stable and reactive boronic ester, facilitating the introduction of benzyl groups into target molecules. Its stability under various conditions makes it a preferred reagent in multi-step synth

Benzylboronic 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, enabling the construction of complex molecules in pharmaceuticals, agrochemicals, and materials science. The compound serves as a stable and reactive boronic ester, facilitating the introduction of benzyl groups into target molecules. Its stability under various conditions makes it a preferred reagent in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds and functional materials due to its efficient reactivity and compatibility with diverse reaction conditions.

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