3-[-(E)-2-Carboxyvinyl]benzeneboronic acid

95%

Reagent Code: #183919
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CAS Number 216144-91-1

science Other reagents with same CAS 216144-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.9764 g/mol
Formula C₉H₉BO₄
badge Registry Numbers
MDL Number MFCD01075738
thermostat Physical Properties
Melting Point 218 °C
Boiling Point 454.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inert gas, dry

description Product Description

Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the production of direct thrombin inhibitors. Its boronic acid group enables reversible binding to serine proteases, making it valuable in targeted enzyme inhibitor design. Also employed in Suzuki-Miyaura cross-coupling reactions for constructing biaryl frameworks in medicinal chemistry. The carboxyvinyl moiety allows further functionalization, facilitating the development of prodrugs or water-soluble derivatives. Commonly applied in research settings for developing boron-containing bioactive molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,760.00
inventory 5g
10-20 days ฿12,320.00
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3-[-(E)-2-Carboxyvinyl]benzeneboronic acid
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Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the production of direct thrombin inhibitors. Its boronic acid group enables reversible binding to serine proteases, making it valuable in targeted enzyme inhibitor design. Also employed in Suzuki-Miyaura cross-coupling reactions for constructing biaryl frameworks in medicinal chemistry. The carboxyvinyl moiety allows further functionalization, facilitating the development of prodrugs or water-soluble derivative

Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the production of direct thrombin inhibitors. Its boronic acid group enables reversible binding to serine proteases, making it valuable in targeted enzyme inhibitor design. Also employed in Suzuki-Miyaura cross-coupling reactions for constructing biaryl frameworks in medicinal chemistry. The carboxyvinyl moiety allows further functionalization, facilitating the development of prodrugs or water-soluble derivatives. Commonly applied in research settings for developing boron-containing bioactive molecules.

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