(3,5-DIFLUOROPYRIDIN-4-YL)BORONIC ACID

95%

Reagent Code: #91817
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CAS Number 956003-87-5

science Other reagents with same CAS 956003-87-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.8986 g/mol
Formula C₅H₄BF₂NO₂
badge Registry Numbers
MDL Number MFCD06246979
thermostat Physical Properties
Boiling Point 261.7℃at 760 mmHg
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of bioactive molecules and in research for drug discovery. Its fluorine substituents enhance its reactivity and stability, making it suitable for specialized applications in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿10,520.00
25mg
10-20 days ฿45,060.00
100mg
10-20 days ฿135,200.00
(3,5-DIFLUOROPYRIDIN-4-YL)BORONIC ACID
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of bioactive molecules and in research for drug discovery. Its fluorine substituents enhance

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing complex molecular structures. Additionally, it is employed in the development of bioactive molecules and in research for drug discovery. Its fluorine substituents enhance its reactivity and stability, making it suitable for specialized applications in medicinal chemistry.

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