Potassium (4-chloro-3-nitrophenyl)trifluoroborate

98%

Reagent Code: #226185
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CAS Number 1218908-71-4

science Other reagents with same CAS 1218908-71-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263 g/mol
Formula C₆H₃BClF₃KNO₂
badge Registry Numbers
MDL Number MFCD12026115
inventory_2 Storage & Handling
Storage 2-8℃, sealed, dried

description Product Description

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its trifluoroborate group provides enhanced stability and controlled reactivity compared to traditional boronic acids, making it suitable for late-stage functionalization and library synthesis in drug discovery. It is also employed in the preparation of substituted biaryls and heterobiaryls, which are common scaffolds in bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿21,300.00
inventory 5g
10-20 days ฿30,110.00
Potassium (4-chloro-3-nitrophenyl)trifluoroborate
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Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its trifluoroborate group provides enhanced stability and controlled reactivity compared to traditional boronic acids, making it suitable for late-stage functionalization and library synthesis in drug discovery. It is also employed in the preparation of substituted biaryls and heterobiaryls, w

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its trifluoroborate group provides enhanced stability and controlled reactivity compared to traditional boronic acids, making it suitable for late-stage functionalization and library synthesis in drug discovery. It is also employed in the preparation of substituted biaryls and heterobiaryls, which are common scaffolds in bioactive compounds.

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