Ethyl 3-(3-amino-4-(methylamino)-N-(pyridin-2-yl)benzamido)propanoate

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Reagent Code: #182107
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CAS Number 212322-56-0

science Other reagents with same CAS 212322-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.39 g/mol
Formula C₁₈H₂₂N₄O₃
badge Registry Numbers
MDL Number MFCD09833624
thermostat Physical Properties
Boiling Point 576.155ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.262 g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for pharmaceutical research. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting inflammatory diseases and certain cancers. The amine and ester functionalities allow for further chemical modifications, enabling optimization of pharmacokinetic properties in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿165.00
inventory 25g
10-20 days ฿560.00
inventory 100g
10-20 days ฿2,180.00
inventory 500g
10-20 days ฿10,670.00

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Ethyl 3-(3-amino-4-(methylamino)-N-(pyridin-2-yl)benzamido)propanoate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for pharmaceutical research. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting inflammatory diseases and certain cancers. The amine and ester functionalities allow for further chemical modifications, enabling optimization of pharmacokinetic properties in drug discovery programs.

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for pharmaceutical research. Its structure supports binding to enzyme active sites, making it valuable in designing drugs targeting inflammatory diseases and certain cancers. The amine and ester functionalities allow for further chemical modifications, enabling optimization of pharmacokinetic properties in drug discovery programs.

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