5-Bromo-6-methyl-3-nitropyridin-2-amine

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Reagent Code: #148353
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CAS Number 68957-50-6

science Other reagents with same CAS 68957-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.04 g/mol
Formula C₆H₆BrN₃O₂
badge Registry Numbers
MDL Number MFCD00091828
thermostat Physical Properties
Boiling Point 316°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.795g/cm3
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure, featuring bromo, nitro, and amino substituents on the pyridine ring, allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine core into larger bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its electron-deficient aromatic ring and reactive substituents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿710.00
inventory 1g
10-20 days ฿1,720.00
inventory 5g
10-20 days ฿6,830.00
inventory 10g
10-20 days ฿11,440.00

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5-Bromo-6-methyl-3-nitropyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure, featuring bromo, nitro, and amino substituents on the pyridine ring, allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine core into larger bioactive molecules. Also utilized in agrochemical research

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure, featuring bromo, nitro, and amino substituents on the pyridine ring, allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine core into larger bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its electron-deficient aromatic ring and reactive substituents.

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