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

98%

Reagent Code: #201164
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CAS Number 2446483-84-5

science Other reagents with same CAS 2446483-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.14 g/mol
Formula C₁₃H₂₃BN₂O₂
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 1-isopropyl-4-methyl-1H-pyrazole moiety into target structures, which can enhance biological activity or modulate physicochemical properties in drug discovery programs. The stability and reactivity profile of this reagent support its use in both small-scale research and late-stage functionalization during development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,930.00
inventory 250mg
10-20 days ฿26,540.00
inventory 1g
10-20 days ฿53,080.00

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1-Isopropyl-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 1-isopropyl-4-methyl-1H-pyrazole moiety into target structures, which can enhance biological activity

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 1-isopropyl-4-methyl-1H-pyrazole moiety into target structures, which can enhance biological activity or modulate physicochemical properties in drug discovery programs. The stability and reactivity profile of this reagent support its use in both small-scale research and late-stage functionalization during development.

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