Ethyl 2-(4-Oxopiperidin-1-Yl)Acetate

95%

Reagent Code: #82329
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CAS Number 145729-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.22 g/mol
Formula C₉H₁₅NO₃
badge Registry Numbers
MDL Number MFCD09936102
thermostat Physical Properties
Boiling Point 289.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.101±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring and an ester group, makes it valuable in the development of drugs targeting neurological and cardiovascular disorders. It is often employed in the synthesis of compounds with potential analgesic, anti-inflammatory, or antihypertensive properties. Additionally, it serves as a building block in the creation of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors or receptor modulators. Its versatility in chemical reactions, such as ester hydrolysis or nucleophilic substitution, allows for its use in diverse synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,148.00
inventory 250mg
10-20 days ฿9,360.00
inventory 1g
10-20 days ฿18,720.00
Ethyl 2-(4-Oxopiperidin-1-Yl)Acetate
This compound is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring and an ester group, makes it valuable in the development of drugs targeting neurological and cardiovascular disorders. It is often employed in the synthesis of compounds with potential analgesic, anti-inflammatory, or antihypertensive properties. Additionally, it serves as a building block in the creation of complex molecules for research in medicinal chemistry, particularly in the design of enzyme inhibitors or receptor modulators. Its versatility in chemical reactions, such as ester hydrolysis or nucleophilic substitution, allows for its use in diverse synthetic pathways.
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