N-Methyl-3-nitropyridin-4-amine

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Reagent Code: #217232
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CAS Number 1633-41-6

science Other reagents with same CAS 1633-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₆H₇N₃O₂
thermostat Physical Properties
Boiling Point 299.5±25.0°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 bioactive molecules. Its structure supports further functionalization, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents. The presence of both nitro and amine groups allows for selective reactions, enabling efficient derivatization in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,640.00
inventory 1g
10-20 days ฿5,480.00
inventory 5g
10-20 days ฿22,280.00

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N-Methyl-3-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 bioactive molecules. Its structure supports further functionalization, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents. The presence of both nitro and amine groups allows for selective reactions, enabling efficient derivatiza

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports further functionalization, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents. The presence of both nitro and amine groups allows for selective reactions, enabling efficient derivatization in multi-step organic syntheses.

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