(4-(azetidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid

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Reagent Code: #89251
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CAS Number 2256708-85-5

science Other reagents with same CAS 2256708-85-5

blur_circular Chemical Specifications

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Weight 245.0060496 g/mol
Formula C₁₀H₁₁BF₃NO₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Its trifluoromethyl group enhances the stability and reactivity of the resulting compounds, making it valuable in the development of bioactive molecules. Additionally, it is employed in the synthesis of potential drug candidates targeting various diseases, including cancer and neurological disorders. Its unique structure also makes it useful in materials science for designing advanced polymers and functional materials.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿53,800.00
inventory 100mg
10-20 days ฿161,400.00
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(4-(azetidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Its trifluoromethyl group enhances the stability and reactivity of the resulting compounds, making it valuable in the development of bioactive molecules. Additionally, it

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Its trifluoromethyl group enhances the stability and reactivity of the resulting compounds, making it valuable in the development of bioactive molecules. Additionally, it is employed in the synthesis of potential drug candidates targeting various diseases, including cancer and neurological disorders. Its unique structure also makes it useful in materials science for designing advanced polymers and functional materials.

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