2-Chloro-4-fluoropyridine-5-boronic acid

95%

Reagent Code: #59366
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CAS Number 2096341-49-8

science Other reagents with same CAS 2096341-49-8

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Weight 175.3531632 g/mol
Formula C₅H₄BClFNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

Used primarily as a building block in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides, while the chloro and fluoro substituents offer further reactivity for functionalization. Commonly employed in the development of bioactive compounds, including potential drug candidates, due to its ability to introduce diverse structural motifs. Also utilized in material science for creating organic electronic components and polymers.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿12,670.00
inventory 25mg
10-20 days ฿26,380.00
inventory 100mg
10-20 days ฿100,240.00

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2-Chloro-4-fluoropyridine-5-boronic acid
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Used primarily as a building block in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides, while the chloro and fluoro substituents offer further reactivity for functionalization. Commonly employed in the development of bioactive compounds,

Used primarily as a building block in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides, while the chloro and fluoro substituents offer further reactivity for functionalization. Commonly employed in the development of bioactive compounds, including potential drug candidates, due to its ability to introduce diverse structural motifs. Also utilized in material science for creating organic electronic components and polymers.

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