3-Carboxyphenylboronic acid

99%

Reagent Code: #90275
label
Alias 3-carboxyphenylboronic acid; m-carboxyphenylboronic acid
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CAS Number 25487-66-5

science Other reagents with same CAS 25487-66-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.94 g/mol
Formula C₇H₇BO₄
badge Registry Numbers
MDL Number MFCD00036833
thermostat Physical Properties
Melting Point 243-247 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. It plays a key role in the development of pharmaceuticals, agrochemicals, and functional materials. Its boronic acid group enables it to act as a receptor for diols and sugars, making it useful in glucose sensing and diagnostic applications. Additionally, it is employed in the preparation of metal-organic frameworks (MOFs) and other advanced materials due to its ability to form stable complexes with metals.

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Test Parameter Specification
Purity (HPLC) 99-100
Melting Point (°C) 240-248
Appearance White to grey powder or crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿450.00
inventory 25g
10-20 days ฿1,390.00
inventory 100g
10-20 days ฿4,820.00

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3-Carboxyphenylboronic acid
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Used in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. It plays a key role in the development of pharmaceuticals, agrochemicals, and functional materials. Its boronic acid group enables it to act as a receptor for diols and sugars, making it useful in glucose sensing and diagnostic applications. Additionally, it is employed in the preparation of metal-organic frameworks (MOFs) and other advanced materials due to its abi

Used in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. It plays a key role in the development of pharmaceuticals, agrochemicals, and functional materials. Its boronic acid group enables it to act as a receptor for diols and sugars, making it useful in glucose sensing and diagnostic applications. Additionally, it is employed in the preparation of metal-organic frameworks (MOFs) and other advanced materials due to its ability to form stable complexes with metals.

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