4-(Benzyloxy)phenylboronic acid

97%

Reagent Code: #90737
label
Alias 4-Benzyloxyphenylboronic acid
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CAS Number 146631-00-7

science Other reagents with same CAS 146631-00-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.05 g/mol
Formula C₁₃H₁₃BO₃
badge Registry Numbers
MDL Number MFCD01075705
thermostat Physical Properties
Melting Point 198-200 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create carbon-carbon bonds in the development of complex organic molecules. Its boronic acid group facilitates efficient coupling with aryl halides, making it essential in the production of drugs, agrochemicals, and advanced materials. Additionally, it finds applications in the synthesis of fluorescent probes and sensors due to its ability to interact with diols and other functional groups.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Solubility in Methanol almost transparent
Appearance White to pale yellow or tan solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿650.00
inventory 250mg
10-20 days ฿260.00
inventory 1g
10-20 days ฿300.00
inventory 25g
10-20 days ฿2,750.00
inventory 100g
10-20 days ฿9,880.00

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4-(Benzyloxy)phenylboronic acid
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create carbon-carbon bonds in the development of complex organic molecules. Its boronic acid group facilitates efficient coupling with aryl halides, making it essential in the production of drugs, agrochemicals, and advanced materials. Additionally, it finds applications in the synthesis of fluorescent probes and sensors due to its ability to interact with diols and other functional groups.
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