N-(4-Methoxybenzyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide

≥95%

Reagent Code: #215566
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CAS Number 2828440-26-0

science Other reagents with same CAS 2828440-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.23 g/mol
Formula C₂₀H₂₅BN₂O₄
thermostat Physical Properties
Boiling Point 559.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex heteroaromatic systems. Commonly applied in the development of bioactive molecules and drug candidates where precise molecular architecture is required. The picolinamide moiety enhances stability and coordination with metal catalysts, improving reaction efficiency. Also employed in medicinal chemistry for late-stage functionalization of drug-like compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,880.00
250mg
10-20 days ฿3,190.00
N-(4-Methoxybenzyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in constructing complex heteroaromatic systems. Commonly applied in the development of bioactive molecules and drug candidates where precise molecular architecture is required. The picolinamide moiety enhances stability and coordination with metal catalysts, improving reaction efficiency. Also employed in medicinal chemistry for late-stage functionalization of drug-like compounds.
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