(3-Hydroxy-4-(methoxycarbonyl)phenyl)boronic acid

98%

Reagent Code: #196834
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CAS Number 1207726-24-6

science Other reagents with same CAS 1207726-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.97 g/mol
Formula C₈H₉BO₅
badge Registry Numbers
MDL Number MFCD18383893
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex aromatic frameworks for drug discovery. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents. Also utilized in the design of sensors and functional materials due to its ability to bind diols and participate in reversible covalent interactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,740.00
inventory 1g
10-20 days ฿4,620.00
inventory 5g
10-20 days ฿16,180.00
inventory 25g
10-20 days ฿61,300.00
(3-Hydroxy-4-(methoxycarbonyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex aromatic frameworks for drug discovery. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents. Also utilized in the design of sensors and functional materials due to its ability

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing complex aromatic frameworks for drug discovery. Commonly employed in the preparation of protease inhibitors and anti-inflammatory agents. Also utilized in the design of sensors and functional materials due to its ability to bind diols and participate in reversible covalent interactions.

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