2-Acetamidopyridine-5-boronic acid pinacol ester

≥95%

Reagent Code: #138091
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CAS Number 904326-87-0

science Other reagents with same CAS 904326-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.11 g/mol
Formula C₁₃H₁₉BN₂O₃
badge Registry Numbers
MDL Number MFCD08690229
thermostat Physical Properties
Melting Point 130-134 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel drug candidates and functional materials. The acetamido group enhances stability and can act as a directing group or participate in further derivatization. Commonly employed in medicinal chemistry for constructing pyridine-containing scaffolds found in kinase inhibitors and other therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,370.00
inventory 1g
10-20 days ฿6,310.00
inventory 5g
10-20 days ฿21,870.00
inventory 25g
10-20 days ฿76,530.00

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2-Acetamidopyridine-5-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 and agrochemical research. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel drug candidates and functional materials. The acetamido group enhances stability and can act as a directing group or participate in further derivatization. Commonly employed in medicinal c

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel drug candidates and functional materials. The acetamido group enhances stability and can act as a directing group or participate in further derivatization. Commonly employed in medicinal chemistry for constructing pyridine-containing scaffolds found in kinase inhibitors and other therapeutic agents.

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