2-Hydroxy-5-(trifluoromethyl)phenylboronicacid

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Reagent Code: #197592
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CAS Number 779329-55-4

science Other reagents with same CAS 779329-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.93 g/mol
Formula C₇H₆BF₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Commonly applied in creating bioactive molecules and functionalized aromatic compounds with enhanced metabolic stability due to the trifluoromethyl group. Also utilized in the preparation of fluorescent probes and sensors, where the hydroxy and boronic acid functionalities allow for selective detection of diols and saccharides.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,050.00
inventory 250mg
10-20 days ฿16,740.00
inventory 1g
10-20 days ฿43,440.00
inventory 500mg
10-20 days ฿27,970.00

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2-Hydroxy-5-(trifluoromethyl)phenylboronicacid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Commonly applied in creating bioactive molecules and functionalized aromatic compounds with enhanced metabolic stability due to the trifluoromethyl group. Also utilized in the preparation of fluorescent probes and sensors, where the hydr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Commonly applied in creating bioactive molecules and functionalized aromatic compounds with enhanced metabolic stability due to the trifluoromethyl group. Also utilized in the preparation of fluorescent probes and sensors, where the hydroxy and boronic acid functionalities allow for selective detection of diols and saccharides.

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