4-(Hydroxymethyl)phenylboronic acid pinacol ester

98%

Reagent Code: #83838
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CAS Number 302348-51-2

science Other reagents with same CAS 302348-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.10 g/mol
Formula C₁₃H₁₉BO₃
badge Registry Numbers
MDL Number MFCD09837617
thermostat Physical Properties
Melting Point 74-80 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and fine chemicals. It is particularly valuable in the production of biaryl compounds, which are essential in drug development and material science. Additionally, it serves as a protecting group for boronic acids, enhancing stability during complex chemical processes. Its application extends to the preparation of sensors and molecular probes due to its reactivity with diols and sugars, making it useful in biochemical research and diagnostic tools.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to Tan Solid, Powder, Crystals and/or Chunks
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿540.00
inventory 5g
10-20 days ฿1,080.00
inventory 25g
10-20 days ฿4,050.00
inventory 100g
10-20 days ฿15,140.00

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4-(Hydroxymethyl)phenylboronic acid pinacol ester
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Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and fine chemicals. It is particularly valuable in the production of biaryl compounds, which are essential in drug development and material science. Additionally, it serves as a protecting group for boronic acids, enhancing stability during complex chemical processes. Its application extends to the preparation of sensors and molecular probes due to

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and fine chemicals. It is particularly valuable in the production of biaryl compounds, which are essential in drug development and material science. Additionally, it serves as a protecting group for boronic acids, enhancing stability during complex chemical processes. Its application extends to the preparation of sensors and molecular probes due to its reactivity with diols and sugars, making it useful in biochemical research and diagnostic tools.

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