5-amino-6-bromopyridine-2-carbonitrile

98%

Reagent Code: #135108
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CAS Number 849353-22-6

science Other reagents with same CAS 849353-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₆H₄BrN₃
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MDL Number MFCD09027188
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for building pyridine-based drug candidates due to its reactive amino and bromo groups, which facilitate coupling reactions and further derivatization. Also utilized in agrochemical research for designing novel pesticides and herbicides.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿7,980.00
inventory 1g
10-20 days ฿19,950.00
inventory 5g
10-20 days ฿82,130.00

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5-amino-6-bromopyridine-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for building pyridine-based drug candidates due to its reactive amino and bromo groups, which facilitate coupling reactions and further derivatization. Al

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for building pyridine-based drug candidates due to its reactive amino and bromo groups, which facilitate coupling reactions and further derivatization. Also utilized in agrochemical research for designing novel pesticides and herbicides.

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