3-Bromo-5-nitropyridin-4-amine

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Reagent Code: #145488
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CAS Number 89284-05-9

science Other reagents with same CAS 89284-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.01 g/mol
Formula C₅H₄BrN₃O₂
thermostat Physical Properties
Melting Point 174-175°C
Boiling Point 346.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, it plays a key role in the preparation of complex heterocyclic systems found in anti-inflammatory, anticancer, and antimicrobial agents. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to interact with biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,520.00
inventory 10g
10-20 days ฿2,520.00
inventory 25g
10-20 days ฿6,050.00
inventory 50g
10-20 days ฿11,680.00

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3-Bromo-5-nitropyridin-4-amine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, it plays a key role in the preparation of complex heterocyclic systems found in anti-inflammatory, anticancer, and antimicro

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, it plays a key role in the preparation of complex heterocyclic systems found in anti-inflammatory, anticancer, and antimicrobial agents. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to interact with biological targets.

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