3-FORMYL-4-METHOXYPHENYLBORONIC ACID

98%

Reagent Code: #90262
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CAS Number 121124-97-8

science Other reagents with same CAS 121124-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD02093661
thermostat Physical Properties
Melting Point 214-217°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its formyl and methoxy groups also provide sites for further functionalization, enhancing its versatility in synthetic chemistry.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿270.00
inventory 5g
10-20 days ฿1,161.00
inventory 25g
10-20 days ฿5,481.00

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3-FORMYL-4-METHOXYPHENYLBORONIC ACID
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it us

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications. Its formyl and methoxy groups also provide sites for further functionalization, enhancing its versatility in synthetic chemistry.

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