1-Cyclopropyl-6-oxo-1,6-dihydropyridine-3-boronic Acid Pinacol Ester

98%

Reagent Code: #192628
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CAS Number 1596367-55-3

science Other reagents with same CAS 1596367-55-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.12 g/mol
Formula C₁₄H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD16996103
thermostat Physical Properties
Boiling Point 326.6±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical development. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and other drug candidates where the pyridine scaffold is essential for target binding. The cyclopropyl group enhances metabolic stability and influences molecular conformation, contributing to improved potency and selectivity in final active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,250.00
inventory 100mg
10-20 days ฿22,080.00
inventory 250mg
10-20 days ฿37,550.00

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1-Cyclopropyl-6-oxo-1,6-dihydropyridine-3-boronic Acid Pinacol Ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical development. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in constructing complex heterocyclic systems. Commonly employed in the preparation of kinase inhibitors and other drug candidates where the pyridine scaffold is essential for target binding. The cyclopropyl group enhances metabolic stability and influences molecular conformation, contributing to improved potency and selectivity in final active compounds.
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