2392-98-5 Usage
Uses
Used in Pharmaceutical Industry:
Salutaridinol is used as a key intermediate compound for the production of important pharmaceutical opioid compounds such as morphine and codeine. Its role in the biosynthetic pathway makes it essential for the synthesis of these drugs, which are widely used for pain management and other medical applications.
Used in Research and Development:
Salutaridinol is used as a subject of study in the field of organic chemistry and pharmaceutical research. Its discovery in the late 20th century has led to ongoing investigations into its properties, synthesis, and potential applications in drug development. This research is crucial for understanding the biosynthesis of opioids and exploring new methods for their production and use.
Check Digit Verification of cas no
The CAS Registry Mumber 2392-98-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2392-98:
(6*2)+(5*3)+(4*9)+(3*2)+(2*9)+(1*8)=95
95 % 10 = 5
So 2392-98-5 is a valid CAS Registry Number.
2392-98-5Relevant academic research and scientific papers
A Regio- and Diastereoselective Anodic Aryl–Aryl Coupling in the Biomimetic Total Synthesis of (?)-Thebaine
Lipp, Alexander,Ferenc, Dorota,Gütz, Christoph,Geffe, Mario,Vierengel, Nina,Schollmeyer, Dieter,Sch?fer, Hans J.,Waldvogel, Siegfried R.,Opatz, Till
supporting information, p. 11055 - 11059 (2018/08/21)
The biosynthesis of thebaine is based on the regioselective, intramolecular, oxidative coupling of (R)-reticuline. For decades, chemists have sought to mimic this coupling by using stoichiometric oxidants. However, all approaches to date have suffered from low yields or the formation of undesired regioisomers. Electrochemistry would represent a sustainable alternative in this respect but all attempts to accomplish an electrochemical synthesis of thebaine have failed so far. Herein, a regio- and diastereoselective anodic coupling of 3′,4′,5′-trioxygenated laudanosine derivatives is presented, which finally enables electrochemical access to (?)-thebaine.
