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

95%

Reagent Code: #226432
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CAS Number 847818-76-2

science Other reagents with same CAS 847818-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.1183 g/mol
Formula C₁₂H₂₁BN₂O₂
badge Registry Numbers
MDL Number MFCD12405508
thermostat Physical Properties
Boiling Point 338 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.03 g/cm3
Storage -20°C, inert atmosphere

description Product Description

Used primarily as a key pyrazole-based intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to incorporate the pyrazole scaffold into pharmaceutical and agrochemical synthesis. Its boronate ester group at the 5-position facilitates efficient and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the development of complex organic molecules, especially in drug discovery for anti-inflammatory, antimicrobial, and CNS-acting agents, as well as materials science, due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,000.00
inventory 250mg
10-20 days ฿1,430.00
inventory 1g
10-20 days ฿4,080.00
inventory 5g
10-20 days ฿14,290.00
1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used primarily as a key pyrazole-based intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to incorporate the pyrazole scaffold into pharmaceutical and agrochemical synthesis. Its boronate ester group at the 5-position facilitates efficient and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the development of complex organic molecules, especially in drug discovery for anti-inflammatory, antimicrobial, a

Used primarily as a key pyrazole-based intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to incorporate the pyrazole scaffold into pharmaceutical and agrochemical synthesis. Its boronate ester group at the 5-position facilitates efficient and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the development of complex organic molecules, especially in drug discovery for anti-inflammatory, antimicrobial, and CNS-acting agents, as well as materials science, due to its stability and reactivity profile.

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