3-Amino-6-Bromopicolinamide

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Reagent Code: #138811
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CAS Number 1660117-37-2

science Other reagents with same CAS 1660117-37-2

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Weight 216.04 g/mol
Formula C₆H₆BrN₃O
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems with potential antiviral, anticancer, and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding affinity in target molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,320.00
inventory 250mg
10-20 days ฿9,110.00
inventory 1g
10-20 days ฿24,270.00
inventory 5g
10-20 days ฿89,370.00

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3-Amino-6-Bromopicolinamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems with potential antiviral, anticancer, and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and he

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic systems. Commonly employed in medicinal chemistry for constructing nitrogen-containing ring systems with potential antiviral, anticancer, and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding affinity in target molecules.

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