4-Carboxyphenylboronic acid

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Reagent Code: #156487
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CAS Number 14047-29-1

science Other reagents with same CAS 14047-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.94 g/mol
Formula C₇H₇BO₄
badge Registry Numbers
MDL Number MFCD00151801
thermostat Physical Properties
Melting Point 220 °C (dec.)(lit.)
Boiling Point 406.4±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.40±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Serves as a key intermediate in the preparation of boron-containing compounds for sensor applications, particularly in glucose detection due to its affinity for diols. Employed in the design of covalent organic frameworks (COFs) and molecular imprinting materials where the carboxylic acid and boronic acid groups allow for dual functionality in self-assembly and recognition processes. Also applied in bioconjugation strategies for labeling biomolecules and in the development of boronic acid-based inhibitors in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿570.00
inventory 25g
10-20 days ฿1,360.00
inventory 100g
10-20 days ฿3,780.00
inventory 500g
10-20 days ฿16,250.00

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4-Carboxyphenylboronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Serves as a key intermediate in the preparation of boron-containing compounds for sensor applications, particularly in glucose detection due to its affinity for diols. Employed in the design of covalent organic frameworks (COFs) and molecular imprinting materials where the carboxylic acid and boronic acid groups allow for

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Serves as a key intermediate in the preparation of boron-containing compounds for sensor applications, particularly in glucose detection due to its affinity for diols. Employed in the design of covalent organic frameworks (COFs) and molecular imprinting materials where the carboxylic acid and boronic acid groups allow for dual functionality in self-assembly and recognition processes. Also applied in bioconjugation strategies for labeling biomolecules and in the development of boronic acid-based inhibitors in medicinal chemistry.

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