Ethyl 3-(benzyl(2-ethoxy-2-oxoethyl)amino)propanoate

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Reagent Code: #184408
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CAS Number 795-18-6

science Other reagents with same CAS 795-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD09833363
thermostat Physical Properties
Boiling Point 135 °C
inventory_2 Storage & Handling
Density 1.092±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its ester and amine functionalities make it suitable for peptide-like chain extensions and the formation of nitrogen-containing heterocycles. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its structural flexibility and ability to mimic natural substrates. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the ethyl ester and benzyl groups can be modified to optimize pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,720.00
inventory 250mg
10-20 days ฿3,290.00
inventory 1g
10-20 days ฿5,890.00
inventory 5g
10-20 days ฿17,250.00

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Ethyl 3-(benzyl(2-ethoxy-2-oxoethyl)amino)propanoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its ester and amine functionalities make it suitable for peptide-like chain extensions and the formation of nitrogen-containing heterocycles. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its structural flexibility and ability to mimic natural substrates. Also utilized in medicinal chemistry for structure-activity relationship (SAR) st

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its ester and amine functionalities make it suitable for peptide-like chain extensions and the formation of nitrogen-containing heterocycles. Commonly employed in the development of enzyme inhibitors and receptor ligands due to its structural flexibility and ability to mimic natural substrates. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, where the ethyl ester and benzyl groups can be modified to optimize pharmacokinetic properties.

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