(1-Isopentyl-1H-pyrazol-5-yl)boronic acid

96%

Reagent Code: #200912
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CAS Number 847818-66-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.03 g/mol
Formula C₈H₁₅BN₂O₂
badge Registry Numbers
MDL Number MFCD12407381
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heteroaryl frameworks found in bioactive compounds. Commonly employed in the development of drug candidates and functional materials due to its reactivity and selectivity in coupling processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,270.00
inventory 1g
10-20 days ฿11,500.00
inventory 5g
10-20 days ฿40,250.00
(1-Isopentyl-1H-pyrazol-5-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heteroaryl frameworks found in bioactive compounds. Commonly employed in the development of drug candidates and functional materials due to its reactivity and selectivity in coupling processes.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heteroaryl frameworks found in bioactive compounds. Commonly employed in the development of drug candidates and functional materials due to its reactivity and selectivity in coupling processes.

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