510-66-7 Usage
Description
(4aS,7aR)-3,4,6,7,7a,8-Hexahydro-12-hydroxy-11-methoxy-7-methyldibenz[d,f]indol-2(5H)-one is a complex chemical compound that belongs to the class of dibenzindolones. It is a derivative of the alkaloid biogen, featuring a dibenzindolone core with a hydroxyl group and a methoxy group attached to it. This unique molecular structure may endow the compound with potential pharmacological or biological activities, although further research is necessary to explore its specific uses and effects.
Uses
Used in Pharmaceutical Industry:
(4aS,7aR)-3,4,6,7,7a,8-Hexahydro-12-hydroxy-11-methoxy-7-methyldibenz[d,f]indol-2(5H)-one is used as a potential pharmaceutical candidate for various applications due to its unique molecular structure and potential pharmacological or biological activities.
Used in Research and Development:
In the field of research and development, (4aS,7aR)-3,4,6,7,7a,8-Hexahydro-12-hydroxy-11-methoxy-7-methyldibenz[d,f]indol-2(5H)-one serves as a subject for further investigation to understand its potential uses and effects in different applications, including its possible role in the development of new drugs or therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 510-66-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 510-66:
(5*5)+(4*1)+(3*0)+(2*6)+(1*6)=47
47 % 10 = 7
So 510-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO3/c1-19-8-7-18-6-5-12(20)10-13(18)16-11(9-15(18)19)3-4-14(22-2)17(16)21/h3-4,10,15,21H,5-9H2,1-2H3
510-66-7Relevant articles and documents
One-pot conversion of thebaine to hydrocodone and synthesis of neopinone ketal
Carroll, Robert J.,Leisch, Hannes,Rochon, Lena,Hudlicky, Tomas,Cox, D. Phillip
experimental part, p. 747 - 752 (2009/07/25)
The ethylene glycol ketal of neopinone was prepared in a one-pot procedure by the reaction of thebaine with ethylene glyocol in the presence of p-toluenesulfonic acid. The ketal is also an intermediate in the conversion of thebaine to hydrocodone with ethylene glycol and Pd(OAc)2, followed by hydrogenation. Additionally, a one-pot procedure for the conversion of thebaine to hydrocodone was achieved by employing palladium catalysis in aqueous medium. Palladium serves a dual purpose in this transformation, first for the activation of the dienol ether of thebaine and second as a hydrogenation catalyst. This procedure was found to be comparable to the two-step protocol which employs diimide reduction of thebaine followed by acid-catalyzed hydrolysis of the resulting 8,14-dihydrothebaine to hydrocodone. Experimental and spectral data are provided for all compounds.