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

≥95%

Reagent Code: #210970
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CAS Number 1105039-88-0

science Other reagents with same CAS 1105039-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.19 g/mol
Formula C₁₇H₂₃BN₂O₃
badge Registry Numbers
MDL Number MFCD16877287
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

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 reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 4-methoxybenzyl-substituted pyrazole moiety into target structures, which can enhance biological activity in drug discovery programs. Its stability and reactivity profile make it suitable for late-stage functionalization in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 250mg
10-20 days ฿1,250.00
inventory 5g
10-20 days ฿17,600.00
inventory 25g
10-20 days ฿85,040.00
inventory 1g
10-20 days ฿4,240.00

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1-(4-Methoxybenzyl)-4-(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 reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 4-methoxybenzyl-substituted pyrazole moiety into target structures, which can enhance biological activity in drug discovery programs. Its stability and reactivity profile make it suitable for late-stage functionalization in multi-step syntheses.
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