1-Isobutyl-3-(trifluoromethyl)pyrazole-5-boronic acid

97%

Reagent Code: #200747
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CAS Number 2304633-89-2

science Other reagents with same CAS 2304633-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.002 g/mol
Formula C₈H₁₂BF₃N₂O₂
badge Registry Numbers
MDL Number MFCD25121750
thermostat Physical Properties
Boiling Point 334.8±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.30±0.1 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of carbon-carbon bonds. This makes it valuable in developing new drug candidates, especially those targeting kinase inhibition and anti-inflammatory agents. The trifluoromethyl and pyrazole moieties contribute to metabolic stability and enhanced binding affinity, while the isobutyl group enhances lipophilicity, aiding in cell membrane permeability. It is also employed in the preparation of novel heterocyclic systems for use in medicinal chemistry and crop protection agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,490.00
inventory 1g
10-20 days ฿13,110.00
inventory 5g
10-20 days ฿48,840.00
1-Isobutyl-3-(trifluoromethyl)pyrazole-5-boronic acid
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of carbon-carbon bonds. This makes it valuable in developing new drug candidates, especially those targeting kinase inhibition and anti-inflammatory agents. The trifluoromethyl and pyrazole moieties contribute to metabolic stability and enhanced binding affi

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of carbon-carbon bonds. This makes it valuable in developing new drug candidates, especially those targeting kinase inhibition and anti-inflammatory agents. The trifluoromethyl and pyrazole moieties contribute to metabolic stability and enhanced binding affinity, while the isobutyl group enhances lipophilicity, aiding in cell membrane permeability. It is also employed in the preparation of novel heterocyclic systems for use in medicinal chemistry and crop protection agents.

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