5-Carboxy-2-ethoxyphenylboronic acid

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Reagent Code: #164150
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CAS Number 1451391-73-3

science Other reagents with same CAS 1451391-73-3

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scatter_plot Molecular Information
Weight 209.99 g/mol
Formula C₉H₁₁BO₅
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MDL Number MFCD11044923
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds for pharmaceutical and agrochemical development. The carboxylic acid group allows for further functionalization or conjugation, while the ethoxy group enhances water solubility and compatibility with various solvents, facilitating reaction control. This combination makes it valuable in the design of active pharmaceutical ingredients (APIs), molecular probes, and special materials such as luminescent or conductive compounds. Its boronic acid moiety enables selective binding to diols, useful in sensor technologies and targeted drug delivery systems. Commonly employed in the preparation of complex intermediates where both coupling and derivatization are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,140.00
inventory 250mg
10-20 days ฿3,650.00
inventory 1g
10-20 days ฿9,890.00

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5-Carboxy-2-ethoxyphenylboronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds for pharmaceutical and agrochemical development. The carboxylic acid group allows for further functionalization or conjugation, while the ethoxy group enhances water solubility and compatibility with various solvents, facilitating reaction control. This combination makes it valuable in the design of active pharmaceutical ingredients (APIs), molecular probes, and special materials such as lumi

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds for pharmaceutical and agrochemical development. The carboxylic acid group allows for further functionalization or conjugation, while the ethoxy group enhances water solubility and compatibility with various solvents, facilitating reaction control. This combination makes it valuable in the design of active pharmaceutical ingredients (APIs), molecular probes, and special materials such as luminescent or conductive compounds. Its boronic acid moiety enables selective binding to diols, useful in sensor technologies and targeted drug delivery systems. Commonly employed in the preparation of complex intermediates where both coupling and derivatization are required.

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