5683-24-9 Usage
Uses
Used in Organic Synthesis:
2,2-Pyrrolidinedicarboxylic acid, 5-oxo-1-phenyl-, diethyl ester is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the formation of diverse chemical entities, contributing to the development of new compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,2-Pyrrolidinedicarboxylic acid, 5-oxo-1-phenyl-, diethyl ester is utilized as a precursor for the synthesis of novel pharmaceutical compounds. Its versatile chemical properties enable the development of new drugs with potential therapeutic benefits.
Used in Drug Delivery Systems:
2,2-Pyrrolidinedicarboxylic acid, 5-oxo-1-phenyl-, diethyl ester has been studied for its potential applications in drug delivery systems. Its unique structure and properties make it a promising candidate for the development of innovative drug delivery platforms, enhancing the efficacy and bioavailability of therapeutic agents.
Used in Antioxidant and Neuroprotective Applications:
Due to its demonstrated antioxidant and neuroprotective properties, 2,2-Pyrrolidinedicarboxylic acid, 5-oxo-1-phenyl-, diethyl ester is a subject of interest for potential therapeutic uses. Its ability to protect cells from oxidative stress and support neuronal health makes it a promising candidate for the development of treatments for various neurological disorders and conditions related to oxidative stress.
Check Digit Verification of cas no
The CAS Registry Mumber 5683-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5683-24:
(6*5)+(5*6)+(4*8)+(3*3)+(2*2)+(1*4)=109
109 % 10 = 9
So 5683-24-9 is a valid CAS Registry Number.
5683-24-9Relevant academic research and scientific papers
Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13)
Kim, Soong-Hoon,Pudzianowski, Andrew T.,Leavitt, Kenneth J.,Barbosa, Joseph,McDonnell, Patricia A.,Metzler, William J.,Rankin, Bruce M.,Liu, Richard,Vaccaro, Wayne,Pitts, William
, p. 1101 - 1106 (2007/10/03)
Computer aided drug design led to a new class of spiro-barbiturates (e.g., 4a, MMP-13 Ki = 4.7 nM) that are potent inhibitors of MMP-13.
Electrochemical Behaviour of ο-Bromoalkanamides. Electrosynthesis of β-, γ-, and δ-Lactams
Casadei, Maria Antonietta,Gessner, Andreas,Inesi, Achille,Jugelt, Werner,Liebezeit, Hannelore,Micheletti Moracci, Franco
, p. 650 - 656 (2007/10/02)
The electrochemical behaviour of bromoamides 1-3 in dimethylformamide solution at a Hg cathode has been investigated by means of cyclic voltammetry at various scan rates and controlled-potential electrolysis.All compounds undergo a facile, high yielding r
