4-Methoxycarbonylphenylboronic

97%

Reagent Code: #90697
label
Alias 4-Methoxyphenylboronic acid; 4-Methoxycarbonylphenylboronic acid
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CAS Number 99768-12-4

science Other reagents with same CAS 99768-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD01632203
thermostat Physical Properties
Melting Point 197-200 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biologically relevant molecules.

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Test Parameter Specification
Purity (HPLC) 97-100%
Purity (Neutralization Titration) 96.5-100%
Appearance Off-white powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,580.00
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿600.00
inventory 100g
10-20 days ฿9,350.00

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4-Methoxycarbonylphenylboronic
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Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biologically rel

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biologically relevant molecules.

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