(1-Isopropyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)boronic acid

98%

Reagent Code: #200757
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CAS Number 1361380-69-9

science Other reagents with same CAS 1361380-69-9

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Weight 221.97 g/mol
Formula C₇H₁₀BF₃N₂O₂
badge Registry Numbers
MDL Number MFCD24448764
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the development of complex molecules with potential therapeutic or pesticidal activity. The presence of trifluoromethyl and isopropyl groups enhances lipophilicity and metabolic stability, making it valuable in medicinal chemistry for optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,150.00
inventory 1g
10-20 days ฿6,310.00
inventory 5g
10-20 days ฿24,210.00

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(1-Isopropyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the development of complex molecules with potential therapeutic or pesticidal activity. The presence of trifluoromethyl and isopropyl groups enhances lipophilicity and metabolic stability, making it valuable in me

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the development of complex molecules with potential therapeutic or pesticidal activity. The presence of trifluoromethyl and isopropyl groups enhances lipophilicity and metabolic stability, making it valuable in medicinal chemistry for optimizing drug candidates.

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