455955-08-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2-PHENYL-PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds due to its versatile reactivity and increased stability provided by the tert-butyl ester group.
Used in Medicinal Applications:
In the field of medicine, 2-PHENYL-PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is used as an anti-inflammatory, antifungal, and antiviral agent, leveraging its potential therapeutic properties to combat various conditions.
Used in Neurodegenerative Disease Treatment:
2-PHENYL-PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is being studied for its potential use in treating neurodegenerative diseases such as Alzheimer's and Parkinson's, where its chemical properties may contribute to disease management and symptom alleviation.
Used in Chemical Processes:
In the chemical industry, 2-PHENYL-PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is used to improve the stability and solubility of compounds in various chemical processes, enhancing the efficiency and effectiveness of these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 455955-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,9,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 455955-08:
(8*4)+(7*5)+(6*5)+(5*9)+(4*5)+(3*5)+(2*0)+(1*8)=185
185 % 10 = 5
So 455955-08-5 is a valid CAS Registry Number.
455955-08-5Relevant articles and documents
SUBSTITUTED PYRROLIDINE AMIDES V
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, (2021/01/22)
The invention relates to compounds according to general formula (I), which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.
Diastereoselective access to enantiomerically pure cis-2,3-disubstituted pyrrolidines
Delaye, Pierre-Olivier,Pradhan, Tanin K.,Lambert, Emilie,Vasse, Jean-Luc,Szymoniak, Jan
experimental part, p. 3395 - 3406 (2010/08/20)
A straightforward access to enantiomerically pure 2,3-disubstituted pyrrolidines is reported that involves diastereoselective allylation of (R)-phenylglycinol-derived imines and a sequential hydrozirconation-cyclization. A number of pyrrolidine derivatives bearing aryl, heteroaryl, alkyl and alkenyl groups have been prepared in this way. Such compounds are useful building blocks in the synthesis of molecules of biological interest, as illustrated by the syntheses of proline derivatives and the naturally occurring alkaloid (-)-isoretronecanol.
3-AMINO-2-PHENYLPYRROLIDINE DERIVATIVES
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Page/Page column 78, (2010/02/14)
3-amino-2-phenylpyrrolidine compounds useful as NK-1 antagonists, with pharmaceutical compositions and methods of treatment comprising same, are disclosed.
