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

97%

Reagent Code: #160711
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CAS Number 1002309-48-9

science Other reagents with same CAS 1002309-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.13 g/mol
Formula C₁₃H₂₁BN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex pyrazole-containing molecules. Commonly applied in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable, crystalline, and compatible with a wide range of functional groups, it supports efficient and selective coupling processes in both research and industrial settings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿2,360.00
inventory 5g
10-20 days ฿9,270.00
inventory 10g
10-20 days ฿17,420.00

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1-Cyclobutyl-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, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex pyrazole-containing molecules. Commonly applied in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable, crystalline, and compat
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex pyrazole-containing molecules. Commonly applied in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable, crystalline, and compatible with a wide range of functional groups, it supports efficient and selective coupling processes in both research and industrial settings.
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