142935-44-2

Usage

Uses

Used in Pharmaceutical Synthesis:
3,3-diethyl-4-oxoazetidin-2-yl propionate is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structural properties allow it to serve as a building block in the creation of new drugs, contributing to the development of novel therapeutic agents.
Used in Medical Research:
In the field of medical research, 3,3-diethyl-4-oxoazetidin-2-yl propionate is explored for its potential applications, including the investigation of its pharmacological properties. Its role in the synthesis of pharmaceuticals makes it a candidate for studies aimed at understanding its interactions with biological systems and its potential therapeutic effects.
Used in Drug Development:
3,3-diethyl-4-oxoazetidin-2-yl propionate is employed in the pharmaceutical industry for drug development. Its unique structural features and potential biological activities position it as a promising candidate for the design and synthesis of innovative drugs, potentially leading to advancements in treatment options for various medical conditions.

Upstream product

• 1189-71-5 isocyanate de chlorosulfonyle 
• 142935-43-1 1-Propionyloxy-2-ethyl-1-butene 

Downstream Products

• 181481-54-9 (4S)-3,3-diethyl-4-{4-[(4-methylpiperazinyl)-carbonyl]phenoxy}azetidin-2-one 
• 157341-41-8 L-694,458 
• 178946-02-6 3.3-Diethyl-4S-(4'-carboxyphenoxy)-2-azetidinone 
• 161281-59-0 (4S)-3,3-diethyl-4-[(4-benzyloxycarbonyl)phenoxy]azetidin-2-one 
• 178946-04-8 (R)-2-[4-(benzyloxycarbonyl)phenoxy]-3,3-diethylazetidin-4-one 
• 204855-17-4 3,3-diethyl-4-{4-[(4-methylpiperazin-1-yl)carbonyl]phenoxy}azetidin-2-one 
• 178946-03-7 (R,S)-2-[4-(benzyloxycarbonyl)phenoxy]-3,3-diethylazetidin-4-one 

Relevant academic research and scientific papers

NOVEL AZETIDINONES USEFUL AS INHIBITORS OF ELASTASE

The invention is directed to novel azetidinones selected from 2-(S)-[4-(((2-(Dimethylamino)ethyl)ethylamino)carbonyl)phenoxy]-3,3-diethyl-N-[1-(R)-(4-(trifluoromethoxy)phenyl)butyl]-4-oxo-1-azetidin ecarboxamide, 2-(S)-[4-(((2-(Dimethylamino)ethyl)ethylam

Process for the preparation of chiral 4-aryloxyazetidinones

A process for preparing a single enantiomer of a 4-aryloxyazetidin-2-one derivative in optically pure form comprises reacting a hindered vinyl ester with chlorosulphonyl isocyanate; displacing the hindered acyloxy group with a phenolic derivative containi