4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)-1H-pyrazole

98%

Reagent Code: #242324
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CAS Number 1218790-40-9

science Other reagents with same CAS 1218790-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.0366 g/mol
Formula C₁₀H₁₄BF₃N₂O₂
badge Registry Numbers
MDL Number MFCD11501039
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. The presence of a trifluoromethyl group enhances the metabolic stability and lipophilicity of resulting products, making it valuable in drug discovery. It is particularly useful in constructing pyrazole-containing scaffolds, which are common in bioactive molecules and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,520.00
inventory 250mg
10-20 days ฿2,490.00
inventory 1g
10-20 days ฿6,450.00
inventory 5g
10-20 days ฿27,910.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)-1H-pyrazole
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Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. The presence of a trifluoromethyl group enhances the metabolic stability and lipophilicity of resulting products, making it valuable in drug discovery. It is particularly useful in constructing pyrazole-containing scaffold

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. The presence of a trifluoromethyl group enhances the metabolic stability and lipophilicity of resulting products, making it valuable in drug discovery. It is particularly useful in constructing pyrazole-containing scaffolds, which are common in bioactive molecules and kinase inhibitors.

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