139014-62-3 Usage
The chemical structure
1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester is a complex molecule that consists of an indole ring with a carboxylic acid group and an ester functionality.
Medicinal properties
Indole derivatives have been investigated for their potential anti-inflammatory, anti-cancer, and anti-microbial activities, so 1H-Indole-3-carboxylic acid,
octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester may also have potential medicinal properties.
Organic synthesis
The presence of the ester functionality may make 1H-Indole-3-carboxylic acid,
octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester useful in organic synthesis as a building block for more complex molecules.
Applications
Due to its potential medicinal properties and usefulness in organic synthesis, 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester has potential applications in both medicinal and synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 139014-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,1 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139014-62:
(8*1)+(7*3)+(6*9)+(5*0)+(4*1)+(3*4)+(2*6)+(1*2)=113
113 % 10 = 3
So 139014-62-3 is a valid CAS Registry Number.
139014-62-3Relevant academic research and scientific papers
PRODUCTION OF DOLASETRON
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Page/Page column 45; 50, (2008/06/13)
The present invention provides an improved process for the preparation of Dolasetron salts, in particularly Dolasetron mesylate. % Also provided are intermediates for the process and methods of preparing the intermediates.
Esters of hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3-(4H)-one and related compounds
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, (2008/06/13)
The present invention is directed to a group of esters of hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(3H)-ones and related compounds. The compounds are prepared from the appropriate carboxylic acids and alcohols by standard procedures or, where steric factors are significant, a new process which makes use of heavy metal salts of super acids can be used. The compounds involved are useful in the treatment of migraine and similar disorders and in cytotoxic drug-induced vomiting.
