3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-b]pyridine

≥95%

Reagent Code: #192803
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CAS Number 1111637-76-3

science Other reagents with same CAS 1111637-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.11 g/mol
Formula C₁₃H₁₈BN₃O₂
badge Registry Numbers
MDL Number MFCD12923385
thermostat Physical Properties
Boiling Point 428.8±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in constructing complex nitrogen-containing heterocycles for drug discovery. Commonly employed in the synthesis of kinase inhibitors and other bioactive molecules due to the pyrazolopyridine scaffold’s favorable pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,600.00
inventory 250mg
10-20 days ฿23,290.00

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3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-b]pyridine
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Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in constructing complex nitrogen-containing heterocycles for drug discovery. Commonly employed in the synthesis of kinase inhibitors and other bioactive molecules due to the pyrazolopyridine scaffold’s favorable pharmacokinetic properties.
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