(3-Chloro-5-(trifluoromethyl)phenyl)boronic acid

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Reagent Code: #90214
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CAS Number 1160561-31-8

science Other reagents with same CAS 1160561-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.37 g/mol
Formula C₇H₅BClF₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex biaryl compounds in pharmaceutical research. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) and agrochemicals. The compound’s trifluoromethyl group enhances the biological activity and metabolic stability of the resulting molecules. Additionally, it is employed in material science for creating advanced organic electronic materials. Its applications also extend to the preparation of ligands for catalysis and functionalized polymers.

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Test Parameter Specification
Appearance Off-white powder
Purity (%) 96.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿333.00
inventory 1g
10-20 days ฿792.00

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(3-Chloro-5-(trifluoromethyl)phenyl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex biaryl compounds in pharmaceutical research. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) and agrochemicals. The compound’s trifluoromethyl group enhances the biological activity and metabolic stability of the resulting molecules. Additionally, it is employed in material science for creating advanced organic electronic materials. Its applications also

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex biaryl compounds in pharmaceutical research. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) and agrochemicals. The compound’s trifluoromethyl group enhances the biological activity and metabolic stability of the resulting molecules. Additionally, it is employed in material science for creating advanced organic electronic materials. Its applications also extend to the preparation of ligands for catalysis and functionalized polymers.

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