1674-01-7 Usage
Description
(7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole is a complex chemical compound featuring a hexahydro-fused indole ring system with an ethyl group at the 5-position. (7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole holds potential pharmaceutical applications due to its unique structure and functional groups, which may exhibit biological activity. Further research and testing are required to determine its specific properties and uses.
Uses
Used in Pharmaceutical Industry:
(7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole is used as a potential pharmaceutical agent for [application reason] due to its unique molecular structure and potential biological activity. The specific application reason would depend on the results of further research and testing, which may reveal its efficacy in treating certain conditions or diseases.
Please note that without more specific information on the compound's properties and potential applications, it is not possible to provide a detailed application reason. (7R)-5-Ethyl-1,4,7,8,9,10-hexahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole's uses would be determined through further research and testing in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1674-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1674-01:
(6*1)+(5*6)+(4*7)+(3*4)+(2*0)+(1*1)=77
77 % 10 = 7
So 1674-01-7 is a valid CAS Registry Number.
1674-01-7Relevant articles and documents
CHIRALITY CONTROL BY KINETIC PROTONATION: ENANTIOSELECTIVE SYNTHESES OF (+)-VELBANAMINE, (-)-ISOVELBANAMINE, AND (+)-CLEAVAMINE
Takano, Seiichi,Uchida, Wataru,Hatakeyama, Susumi,Ogasawara, Kunio
, p. 733 - 736 (2007/10/02)
Optimal conditions for inversion of chirality at 2-position of the 2-alkyllactone(5) have been established.By utilizing the inversion method developed, three indole alkaloids, (+)-velbanamine(16), (-)-isovelbanamine(17), and (+)-cleavamine(18), have been synthesized from the chiral lactone(1) which has been previously used for the syntheses of the enantiomers of these alkaloids.
