3-(Pyrazin-2-yl)-5-trifluoromethylphenylboronic acid

95%

Reagent Code: #91862
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CAS Number 2225180-54-9

science Other reagents with same CAS 2225180-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.9996296 g/mol
Formula C₁₁H₈BF₃N₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs targeting various diseases, such as cancer and inflammation. Additionally, it is utilized in material science for creating advanced polymers and electronic materials. Its trifluoromethyl group enhances the stability and reactivity of the resulting compounds, making it a versatile building block in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿13,400.00
inventory 25mg
10-20 days ฿40,200.00
inventory 100mg
10-20 days ฿120,600.00

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3-(Pyrazin-2-yl)-5-trifluoromethylphenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs targeting various diseases, such as cancer and inflammation. Additionally, it is utilized in material

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs targeting various diseases, such as cancer and inflammation. Additionally, it is utilized in material science for creating advanced polymers and electronic materials. Its trifluoromethyl group enhances the stability and reactivity of the resulting compounds, making it a versatile building block in research and industrial applications.

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