2-Hydroxyphenylboronic acid pinacol ester

97%

Reagent Code: #89870
label
Alias 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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CAS Number 269409-97-4

science Other reagents with same CAS 269409-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.07 g/mol
Formula C₁₂H₁₇BO₃
badge Registry Numbers
MDL Number MFCD02093754
thermostat Physical Properties
Boiling Point 282 °C(lit.)
inventory_2 Storage & Handling
Density 1.05 g/mL at 25 °C(lit.)
Storage Room temperature, sealed, dry

description Product Description

2-Hydroxyphenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing biaryl compounds. Its boronic ester group facilitates efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other biological molecules, enabling applications in biochemical research and diagnostics. The compound’s stability and reactivity also make it suitable for use in polymer chemistry and material science for modifying surfaces or creating functionalized polymers.

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Test Parameter Specification
Purity 96.5-100%
Appearance colorless liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿342.00
inventory 5g
10-20 days ฿1,566.00

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2-Hydroxyphenylboronic acid pinacol ester
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2-Hydroxyphenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing biaryl compounds. Its boronic ester group facilitates efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other biologic

2-Hydroxyphenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing biaryl compounds. Its boronic ester group facilitates efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other biological molecules, enabling applications in biochemical research and diagnostics. The compound’s stability and reactivity also make it suitable for use in polymer chemistry and material science for modifying surfaces or creating functionalized polymers.

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