64643-72-7 Usage
Description
(5alpha)-17-(cyclobutylcarbonyl)-4,5-epoxy-14-hydroxy-3-methoxymorphinan-6-one is a complex organic molecule with a morphinan skeleton, featuring a cyclobutylcarbonyl group on the 17th carbon, a 4,5-epoxy ring, a hydroxy group at the 14th carbon, and a methoxy group at the 3rd carbon. (5alpha)-17-(cyclobutylcarbonyl)-4,5-epoxy-14-hydroxy-3-methoxymorphinan-6-one is likely to exhibit opioid-like properties due to its morphinan structure, suggesting potential pharmacological applications as an analgesic or in the treatment of opioid addiction. Further research and testing are required to fully comprehend its chemical properties and potential biological activity.
Uses
Used in Pharmaceutical Industry:
(5alpha)-17-(cyclobutylcarbonyl)-4,5-epoxy-14-hydroxy-3-methoxymorphinan-6-one is used as a potential analgesic for the treatment of pain due to its opioid-like properties stemming from its morphinan structure.
Used in Addiction Treatment:
(5alpha)-17-(cyclobutylcarbonyl)-4,5-epoxy-14-hydroxy-3-methoxymorphinan-6-one is used as a potential therapeutic agent for the treatment of opioid addiction, leveraging its morphinan structure to help manage withdrawal symptoms and reduce cravings.
Check Digit Verification of cas no
The CAS Registry Mumber 64643-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,4 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64643-72:
(7*6)+(6*4)+(5*6)+(4*4)+(3*3)+(2*7)+(1*2)=137
137 % 10 = 7
So 64643-72-7 is a valid CAS Registry Number.
64643-72-7Relevant articles and documents
A New Reagent for the Selective, High-Yield N-Dealkylation of Tertiary Amines: Improved Syntheses of Naltrexone and Nalbuphine
Olofson, R. A.,Martz, Jonathan T.,Senet, Jean-Pierre,Piteau, Marc,Malfroot, Thierry
, p. 2081 - 2082 (2007/10/02)
Secondary amine hydrochlorides are obtained in high yield by reaction of tertiary amines with α-chloroethyl chloroformate followed by warming the intermediate carbamate in methanol.
