74572-00-2 Usage
Uses
Used in Medicinal Chemistry:
R-BPM is used as a building block for the synthesis of pharmaceuticals and bioactive compounds due to its unique structure and pharmacological properties. Its versatility allows for the development of new drugs with potential therapeutic applications.
Used in Pharmaceutical Industry:
R-BPM is used as an analgesic and anti-inflammatory agent, exhibiting potential activity in alleviating pain and reducing inflammation. Its pharmacological properties make it a valuable compound for the development of new medications to treat various conditions.
Used in Chiral Resolution:
R-BPM is used as a chiral resolving agent in chromatography, a technique used to separate enantiomers (mirror-image isomers) of chiral compounds. Its ability to selectively interact with enantiomers makes it a valuable tool in the analysis and purification of chiral substances.
Used in Asymmetric Catalysis:
R-BPM is used as a ligand in asymmetric catalysis, a process that involves the selective transformation of prochiral molecules into chiral products with the help of a chiral catalyst. Its unique structure and properties make it a promising candidate for enhancing the efficiency and selectivity of catalytic reactions in the synthesis of enantiomerically pure compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 74572-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,7 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74572-00:
(7*7)+(6*4)+(5*5)+(4*7)+(3*2)+(2*0)+(1*0)=132
132 % 10 = 2
So 74572-00-2 is a valid CAS Registry Number.
74572-00-2Relevant academic research and scientific papers
Synthesis of enantiopure 1,4-dioxanes, morpholines, and piperazines from the reaction of chiral 1,2-diols, amino alcohols, and diamines with vinyl selenones
Bagnoli, Luana,Scarponi, Catalina,Rossi, Maria Giovanna,Testaferri, Lorenzo,Tiecco, Marcello
supporting information; experimental part, p. 993 - 999 (2011/03/20)
The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-aminoalcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedu
SYNTHESIS AND ABSOLUTE CONFIGURATION OF SUBSTITUTED MORPHOLINES
Bettoni, Giancarlo,Franchini, Carlo,Perrone, Roberto,Tortorella, Vincenzo
, p. 409 - 415 (2007/10/02)
We studied methods of stereospecific synthesis that enabled us to obtain variously substituted morpholinic compounds and to determine their absolute configuration.From a study of the chiroptical properties of synthetic N-(2-pyridyl-N-oxide) derivatives of optically active morpholines, it was possible to correlate the sign of the Cotton effect with the absolute configuration.This correlation agrees with that previously established for derivatives of the piperidine type.By evaluating the various contributions to the Cotton effect of substituents in positions 2 and 3, we established the absolute configuration of bicyclic compounds condensed in the two positions mentioned above.
