1-(Difluoromethyl)-3-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-1H-pyrazole

97%

Reagent Code: #177939
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CAS Number 2173194-53-9

science Other reagents with same CAS 2173194-53-9

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Weight 244.05 g/mol
Formula C₁₀H₁₅BF₂N₂O₂
badge Registry Numbers
MDL Number MFCD30181542
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing bioactive molecules. Commonly employed in the development of fungicides, herbicides, and medicinal compounds targeting inflammation and central nervous system disorders. Its difluoromethyl group enhances metabolic stability and lipophilicity, improving drug candidate performance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,070.00
inventory 250mg
10-20 days ฿4,140.00
inventory 1g
10-20 days ฿11,180.00

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1-(Difluoromethyl)-3-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-1H-pyrazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing bioactive molecules. Commonly employed in the development of fungicides, herbicides, and medicinal compounds targeting inflammation and central nervous system disorders. Its difluoromethyl group enhances

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole derivatives in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing bioactive molecules. Commonly employed in the development of fungicides, herbicides, and medicinal compounds targeting inflammation and central nervous system disorders. Its difluoromethyl group enhances metabolic stability and lipophilicity, improving drug candidate performance.

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