N,N-DIethyl-6-methyl-5-nitro-2-pyridinamine

95%

Reagent Code: #218927
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CAS Number 28489-43-2

science Other reagents with same CAS 28489-43-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.25 g/mol
Formula C₁₀H₁₅N₃O₂
badge Registry Numbers
MDL Number MFCD11974904
thermostat Physical Properties
Boiling Point 331.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.151±0.06 g/cm3(Predicted)
Storage Room temperature, dry, inert atmosphere

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiprotozoal agents. It serves as a key building block in the production of drugs targeting parasitic infections such as giardiasis and trichomoniasis. Its nitro group and amine functionality allow for further chemical modifications, enabling the creation of biologically active compounds. Also employed in research settings for structure-activity relationship studies in medicinal chemistry due to its pyridine-based scaffold.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿1,900.00
inventory 5g
10-20 days ฿6,410.00

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N,N-DIethyl-6-methyl-5-nitro-2-pyridinamine
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiprotozoal agents. It serves as a key building block in the production of drugs targeting parasitic infections such as giardiasis and trichomoniasis. Its nitro group and amine functionality allow for further chemical modifications, enabling the creation of biologically active compounds. Also employed in research settings for structure-activity relationship studies in medicinal chemistry due to its

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiprotozoal agents. It serves as a key building block in the production of drugs targeting parasitic infections such as giardiasis and trichomoniasis. Its nitro group and amine functionality allow for further chemical modifications, enabling the creation of biologically active compounds. Also employed in research settings for structure-activity relationship studies in medicinal chemistry due to its pyridine-based scaffold.

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