634196-86-4 Usage
Uses
Used in Pharmaceutical Research and Development:
(S)-2-((S)-3-(4-(benzyloxy)phenyl)-2-oxopyrrolidin-1-yl)-4-methylpentanoic acid is used as a potential drug candidate in pharmaceutical research and development due to its structural similarity to biologically active compounds. Its unique molecular configuration may confer it with therapeutic effects that could be beneficial in treating various medical conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-2-((S)-3-(4-(benzyloxy)phenyl)-2-oxopyrrolidin-1-yl)-4-methylpentanoic acid is utilized for the exploration of its potential as a lead compound. Its chemical properties and interactions with biological targets are studied to assess its viability for the development of new medications, particularly those with anti-inflammatory or analgesic capabilities.
Used in Drug Design and Optimization:
(S)-2-((S)-3-(4-(benzyloxy)phenyl)-2-oxopyrrolidin-1-yl)-4-methylpentanoic acid serves as a foundation for drug design and optimization processes. Its molecular structure is analyzed and modified to enhance its pharmacological properties, such as potency, selectivity, and bioavailability, with the aim of creating more effective and safer drugs.
Note: Since the provided materials do not specify particular applications or industries for (S)-2-((S)-3-(4-(benzyloxy)phenyl)-2-oxopyrrolidin-1-yl)-4-methylpentanoic acid, the uses listed are general and based on the potential inferred from its molecular structure and the nature of similar compounds in pharmaceutical contexts. Further research would be necessary to identify specific applications and industries where (S)-2-((S)-3-(4-(benzyloxy)phenyl)-2-oxopyrrolidin-1-yl)-4-methylpentanoic acid could be effectively utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 634196-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,1,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 634196-86:
(8*6)+(7*3)+(6*4)+(5*1)+(4*9)+(3*6)+(2*8)+(1*6)=174
174 % 10 = 4
So 634196-86-4 is a valid CAS Registry Number.
634196-86-4Relevant academic research and scientific papers
Quaternary chiral center via diastereoselective enolate amination enables the synthesis of an anti-inflammatory agent
Magnus, Nicholas A.,Campagna, Silvio,Confalone, Pat N.,Savage, Scott,Meloni, David J.,Waltermire, Robert E.,Wethman, Robert G.,Yates, Mathew
experimental part, p. 159 - 167 (2010/04/29)
The D-leucine amino acid residue necessary for the synthesis of BMS-561392,1, was employed as a chiral directing group for a diastereoselective enolate animation to establish the quaternary chiral center. Enhanced diastereomeric ratios were observed while conducting the enolate amination with 1-chloro-1-nitrosocyclo- pentane 6 in the presence of LiCl. Analogies are drawn between known tertiary amide amino alcohol chiral auxiliaries which have been used to effect diastereoselective enolate alkylations and aminations. Once the stereochemical features of 1 were established, an efficient reaction sequence was devised to complete its synthesis. During the course of this research, accelerated reaction calorimetry (ARC) data substantiated that the aminating agent 1-chloro-1- nitrosocyclopentane 6 was not safe to use as a neat compound. Consequently, a preparation and use of 6 as a stock solution in methyl tert-butyl ether (MTBE) was developed that rendered it safe for use.
ASYMETRIC SYNTHESIS OF AMINO-PYRROLIDINONES
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Page 36, (2010/02/04)
A novel process for the asymmetric synthesis of an amino-pyrrolidinone of the type shown below from appropriate pyrrolidinones is described. [Insert Chemical Formula] These compounds are useful as intermediates for MMP and TACE inhibitors.
