3-Carboxy-5-nitrophenylboronic acid

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Reagent Code: #90274
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Alias 3-Carboxy-5-nitrophenylboronic acid
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CAS Number 101084-81-5

science Other reagents with same CAS 101084-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.94 g/mol
Formula C₇H₆BNO₆
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MDL Number MFCD00757433
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical and materials research. The nitro and carboxyl groups enhance its reactivity and solubility, enabling precise modifications in target molecules. It is also employed in the development of sensors and probes for detecting biological molecules due to its ability to interact with diols and other functional groups. Additionally, it serves as a building block in the synthesis of advanced polymers and catalysts.

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Test Parameter Specification
Purity (HPLC) 97-100
Melting point 248-252
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿920.00
inventory 5g
10-20 days ฿2,640.00
inventory 25g
10-20 days ฿11,500.00

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3-Carboxy-5-nitrophenylboronic acid
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Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical and materials research. The nitro and carboxyl groups enhance its reactivity and solubility, enabling precise modifications in target molecules. It is also employed in the development of sensors and probes for detecting biological molecules due to its ability to

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical and materials research. The nitro and carboxyl groups enhance its reactivity and solubility, enabling precise modifications in target molecules. It is also employed in the development of sensors and probes for detecting biological molecules due to its ability to interact with diols and other functional groups. Additionally, it serves as a building block in the synthesis of advanced polymers and catalysts.

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