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

95%

Reagent Code: #202919
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CAS Number 1396123-92-4

science Other reagents with same CAS 1396123-92-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.06 g/mol
Formula C₁₁H₁₆BF₃N₂O₂
badge Registry Numbers
MDL Number MFCD28368565
thermostat Physical Properties
Boiling Point 320.4±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biologically active pyrazole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The presence of trifluoromethyl and methyl groups enhances electronic and metabolic stability in final compounds, often leading to improved bioactivity. Commonly applied in the development of medicinal candidates targeting inflammation, cancer, and central nervous system disorders.

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inventory 100mg
10-20 days ฿18,510.00

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1-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-1H-pyrazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biologically active pyrazole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The presence of trifluoromethyl and methyl groups enhances electronic and metabolic stability in final compounds, often leading to improved bioactivity. Commonly applied in the development of medicinal candidates targeting inflammation, cancer, a

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biologically active pyrazole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. The presence of trifluoromethyl and methyl groups enhances electronic and metabolic stability in final compounds, often leading to improved bioactivity. Commonly applied in the development of medicinal candidates targeting inflammation, cancer, and central nervous system disorders.

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