4-Fluoro-2-(3-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid

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Reagent Code: #92142
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CAS Number 2225175-45-9

science Other reagents with same CAS 2225175-45-9

blur_circular Chemical Specifications

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Weight 220.9960632 g/mol
Formula C₉H₉BFN₃O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily used in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic compounds, especially in the pharmaceutical industry. Its boronic acid group makes it highly valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and advanced materials. Additionally, its pyrazole and pyridine moieties contribute to its utility in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its applications extend to the development of new therapeutic agents and functional materials due to its structural versatility.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,520.00
inventory 25mg
10-20 days ฿45,060.00
inventory 100mg
10-20 days ฿135,200.00

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4-Fluoro-2-(3-methyl-1H-pyrazol-1-yl)pyridine-5-boronic acid
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This chemical is primarily used in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic compounds, especially in the pharmaceutical industry. Its boronic acid group makes it highly valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and advanced materials. Additionally, its pyrazole and pyridine moieties contribute to its uti

This chemical is primarily used in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic compounds, especially in the pharmaceutical industry. Its boronic acid group makes it highly valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and advanced materials. Additionally, its pyrazole and pyridine moieties contribute to its utility in designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Its applications extend to the development of new therapeutic agents and functional materials due to its structural versatility.

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