572923-00-3 Usage
Uses
Used in Pharmaceutical Industry:
(S)-4-(4-ISOPROPYL-2-OXOOXAZOLIDIN-3-YL)BENZALDEHYDE is used as a building block for the synthesis of pharmaceutical compounds due to its unique chemical structure and potential applications in drug development.
Used in Research and Development:
In the field of research and development, (S)-4-(4-ISOPROPYL-2-OXOOXAZOLIDIN-3-YL)BENZALDEHYDE serves as a valuable compound for exploring new chemical reactions and understanding its properties, which can contribute to the advancement of pharmaceutical sciences.
Used in Laboratory Settings:
As a compound with potential pharmaceutical applications, (S)-4-(4-ISOPROPYL-2-OXOOXAZOLIDIN-3-YL)BENZALDEHYDE is used in laboratory settings for conducting experiments, testing its reactivity, and evaluating its effectiveness in the synthesis of target pharmaceutical compounds. Proper safety measures must be followed to ensure the safe handling of (S)-4-(4-ISOPROPYL-2-OXOOXAZOLIDIN-3-YL)BENZALDEHYDE.
Check Digit Verification of cas no
The CAS Registry Mumber 572923-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,2,9,2 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 572923-00:
(8*5)+(7*7)+(6*2)+(5*9)+(4*2)+(3*3)+(2*0)+(1*0)=163
163 % 10 = 3
So 572923-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c1-9(2)12-8-17-13(16)14(12)11-5-3-10(7-15)4-6-11/h3-7,9,12H,8H2,1-2H3/t12-/m1/s1
572923-00-3Relevant academic research and scientific papers
Ghosh, Arun,Sieser, Janice E.,Riou, Maxime,Cai, Weiling,Rivera-Ruiz, Luis
, p. 2207 - 2210 (2003)
(Matrix presented) An efficient method for intermolecular N-arylation of oxazolidinones using Pd2dba3 and various phosphine ligands in the presence of a weak base is reported. The conditions allow the use of cheaper aryl chlorides containing functionalities such as enolizable ketones, amides, etc., which would be incompatible with other coupling methods. The coupling reaction can be used to prepare enantiopure N-aryl β-amino alcohols. Depending on the stereoelectronic nature of the aryl chloride, careful choice of ligand was necessary for the success of these reactions.
