Phenylboronic acid neopentylglycol ester

97%

Reagent Code: #91215
label
Alias 5,5-Dimethyl-2-phenyl-1,3,2-dioxaborinane Neopentyl glycol phenylboronate
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CAS Number 5123-13-7

science Other reagents with same CAS 5123-13-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.05 g/mol
Formula C₁₁H₁₅BO₂
badge Registry Numbers
MDL Number MFCD05663851
thermostat Physical Properties
Melting Point 62-66 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Phenylboronic acid neopentylglycol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and efficient boron reagent for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability and solubility in organic solvents make it a preferred choice for catalytic processes. Additionally, it is employed in the preparation of functional materials, such as polymers and sensors, due to its ability to interact with diols and other Lewis bases. Its role in medicinal chemistry is notable for creating bioactive compounds and drug intermediates.

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Test Parameter Specification
Carbon 67.1-72%
Melting point 62-66
Purity (HPLC) 97-100%
Appearance White to brown crystals or powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,210.00
inventory 25g
10-20 days ฿4,260.00
inventory 100g
10-20 days ฿12,840.00

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Phenylboronic acid neopentylglycol ester
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Phenylboronic acid neopentylglycol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and efficient boron reagent for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability and solubility in organic solvents make it a preferred choice for catalytic processes. Additionally, it is employed in the preparation of functional materials, such as polymers an

Phenylboronic acid neopentylglycol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and efficient boron reagent for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability and solubility in organic solvents make it a preferred choice for catalytic processes. Additionally, it is employed in the preparation of functional materials, such as polymers and sensors, due to its ability to interact with diols and other Lewis bases. Its role in medicinal chemistry is notable for creating bioactive compounds and drug intermediates.

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