3-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine

98%

Reagent Code: #241631
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CAS Number 864754-21-2

science Other reagents with same CAS 864754-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.15 g/mol
Formula C₁₅H₂₀BN₃O₂
badge Registry Numbers
MDL Number MFCD08706029
thermostat Physical Properties
Boiling Point 450.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.12g/cm3
Storage Room temperature, dry and sealed from light

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 pharmaceutical and agrochemical synthesis. Its pyrazole and pyridine moieties make it valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. It is also employed in the development of functional materials, including organic semiconductors and ligands for catalysis. The boronate ester group allows for efficient and mild coupling with aryl halides, making it suitable for late-stage functionalization in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿600.00
inventory 250mg
10-20 days ฿1,310.00
inventory 1g
10-20 days ฿5,200.00
inventory 5g
10-20 days ฿25,920.00

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3-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine
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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 pharmaceutical and agrochemical synthesis. Its pyrazole and pyridine moieties make it valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. It is also employed in the development of functional materials, including organic semiconductors and ligands for catalysis. The boronate ester group allows for efficient and mild co

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole and pyridine moieties make it valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. It is also employed in the development of functional materials, including organic semiconductors and ligands for catalysis. The boronate ester group allows for efficient and mild coupling with aryl halides, making it suitable for late-stage functionalization in drug discovery.

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