634196-85-3 Usage
Uses
Used in Organic Synthesis:
Methyl 2-(4-(benzyloxy)phenyl)-4-oxobutanoate is used as a key intermediate in organic synthesis for the preparation of various chemical compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, methyl 2-(4-(benzyloxy)phenyl)-4-oxobutanoate is employed as a building block for the development of pharmaceuticals. Its structural features allow for the creation of new compounds with potential therapeutic properties, contributing to the advancement of drug discovery and design.
Used in Pharmaceutical Industry:
Methyl 2-(4-(benzyloxy)phenyl)-4-oxobutanoate is used as a precursor in the pharmaceutical industry for the synthesis of biologically active molecules. Its diverse applications and compatibility with various chemical reactions facilitate the production of innovative drugs with potential health benefits.
Used in Research and Development:
In research and development settings, methyl 2-(4-(benzyloxy)phenyl)-4-oxobutanoate is utilized as a versatile compound for exploring new chemical reactions and pathways. Its unique structure and reactivity provide opportunities for scientists to investigate novel approaches in chemical synthesis and compound development.
Check Digit Verification of cas no
The CAS Registry Mumber 634196-85-3 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 634196-85:
(8*6)+(7*3)+(6*4)+(5*1)+(4*9)+(3*6)+(2*8)+(1*5)=173
173 % 10 = 3
So 634196-85-3 is a valid CAS Registry Number.
634196-85-3Relevant 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 34-35, 46-47, (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.
