352534-92-0 Usage
Description
(S)-4,5,5-triphenyl-oxazolidin-2-one is a chiral chemical compound belonging to the oxazolidinone class. It features a unique three-dimensional structure that serves as a chiral auxiliary in organic synthesis, playing a crucial role in controlling the stereochemistry of chemical reactions. (S)-4,5,5-triphenyl-oxazolidin-2-one is highly valued for its structural integrity and stability, making it an essential component in the creation of complex organic molecules with specific stereochemical properties.
Uses
Used in Pharmaceutical Synthesis:
(S)-4,5,5-triphenyl-oxazolidin-2-one is used as a building block for the synthesis of various pharmaceutical and biologically active compounds. Its ability to control stereochemistry makes it a valuable asset in the development of new drugs with improved efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-4,5,5-triphenyl-oxazolidin-2-one is employed as a chiral auxiliary to guide the stereochemical outcome of reactions. This helps in the production of enantiomerically pure compounds, which are essential for the development of effective and safe medications.
Used in Research and Development:
(S)-4,5,5-triphenyl-oxazolidin-2-one is also utilized in research and development for the study of stereoselective reactions and the exploration of new synthetic pathways. Its high structural integrity and stability make it an ideal candidate for investigating the mechanisms of various chemical processes and for designing novel synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 352534-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 352534-92:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*4)+(2*9)+(1*2)=140
140 % 10 = 0
So 352534-92-0 is a valid CAS Registry Number.
352534-92-0Relevant articles and documents
Synthesis and application of N-3,5-dinitrobenzoyl and C3 symmetric diastereomeric chiral stationary phases
Ryoo, Jae Jeong,Yu, Jeong Jae
, (2022/01/20)
Three diastereomeric chiral compounds, namely, (R,R)-(+)-2-amino-1,2-diphenylethanol, (1S,2R)-(+)-2-amino-1,2-diphenylethanol, and (1R,2R)-(+)-1,2-diphenylethylenediamine were used as starting materials for preparing three N-3,5-dinitrobenzoyl derivative
Parallel kinetic resolution of D-labelled 2-aryl-propionic and butanoic acids using quasi-enantiomeric combinations of oxazolidin-2-ones
Coulbeck, Elliot,Dingjan, Marco,Eames, Jason
experimental part, p. 193 - 205 (2010/11/18)
The parallel kinetic resolution of racemic 2-aryl-2-deuterio-propionic and butanoic acids using an equimolar combination of quasi-enantiomeric oxazolidin-2-ones is discussed. The levels of diastereoselectivity were high leading to enantiomerically pure D-
