3-Chloro-2-(trifluoromethoxy)phenylboronicacid

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Reagent Code: #166207
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CAS Number 1942072-67-4

science Other reagents with same CAS 1942072-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.37 g/mol
Formula C₇H₅BClF₃O₃
badge Registry Numbers
MDL Number MFCD18393881
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, 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 for building complex aromatic structures. Commonly applied in the development of bioactive molecules, including antifungal, anti-inflammatory, and herbicidal compounds. The presence of chlorine and trifluoromethoxy groups enhances reactivity and influences the electronic properties of the final product, improving metabolic stability and target binding in medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,900.00
inventory 250mg
10-20 days ฿6,120.00
inventory 1g
10-20 days ฿16,420.00

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3-Chloro-2-(trifluoromethoxy)phenylboronicacid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, 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 for building complex aromatic structures. Commonly applied in the development of bioactive molecules, including antifungal, anti-inflammatory, and herbicidal compounds. The presence of chlorine and trifluoromethoxy groups enhances react

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, 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 for building complex aromatic structures. Commonly applied in the development of bioactive molecules, including antifungal, anti-inflammatory, and herbicidal compounds. The presence of chlorine and trifluoromethoxy groups enhances reactivity and influences the electronic properties of the final product, improving metabolic stability and target binding in medicinal chemistry applications.

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