(5-(Ethoxycarbonyl)-6-methylpyridin-3-yl)boronic acid

95%

Reagent Code: #130115
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CAS Number 2291165-09-6

science Other reagents with same CAS 2291165-09-6

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Weight 209.01 g/mol
Formula C₉H₁₂BNO₄
inventory_2 Storage & Handling
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 pharmaceuticals and biologically active compounds. Its boronic acid functionality enables efficient carbon-carbon bond formation, particularly in the development of pyridine-based drug candidates. Commonly applied in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. The ethoxycarbonyl and methyl substituents enhance reactivity and selectivity in coupling processes, making it valuable in the preparation of complex heterocyclic systems found in agrochemicals and functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,240.00
inventory 1g
10-20 days ฿26,600.00
inventory 100mg
10-20 days ฿6,020.00

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(5-(Ethoxycarbonyl)-6-methylpyridin-3-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and biologically active compounds. Its boronic acid functionality enables efficient carbon-carbon bond formation, particularly in the development of pyridine-based drug candidates. Commonly applied in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. The ethoxycarbonyl and methyl substituents enhance reactivity and selectivity in coupling processes, making it valua

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and biologically active compounds. Its boronic acid functionality enables efficient carbon-carbon bond formation, particularly in the development of pyridine-based drug candidates. Commonly applied in medicinal chemistry for constructing kinase inhibitors and other targeted therapies. The ethoxycarbonyl and methyl substituents enhance reactivity and selectivity in coupling processes, making it valuable in the preparation of complex heterocyclic systems found in agrochemicals and functional materials.

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