2292-20-8 Usage
Description
5,7,8,14-Tetrahydro-3,4,10,11-tetramethoxy-6-methyldibenz[c,g]azecin-13(6H)-one, also known as cryptopalmine, is an alkaloid found in Papaver nudicaule L. and Argemone munita Dur. & Hilg. subsp. rotunda. It forms clusters of colorless crystals when crystallized from Me2CO and has a crystalline hydriodide with a melting point of 176-177°C (dec.) and a methiodide with a melting point of 192-194°C. The structure of this compound has been deduced from its mass spectrum and confirmed by synthesis.
Uses
Used in Pharmaceutical Industry:
5,7,8,14-Tetrahydro-3,4,10,11-tetramethoxy-6-methyldibenz[c,g]azecin-13(6H)-one is used as a pharmaceutical compound for its potential therapeutic applications. The alkaloid's unique structure and properties make it a candidate for further research and development in the field of medicine.
Used in Chemical Research:
5,7,8,14-Tetrahydro-3,4,10,11-tetramethoxy-6-methyldibenz[c,g]azecin-13(6H)-one is also used in chemical research as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups can be exploited to create new compounds with potential applications in various industries.
Used in Analytical Chemistry:
5,7,8,14-Tetrahydro-3,4,10,11-tetramethoxy-6-methyldibenz[c,g]azecin-13(6H)-one can be used in analytical chemistry for the development of new methods and techniques for the identification and quantification of similar alkaloids in natural sources or synthesized products.
Used in Toxicology Studies:
Due to its occurrence in certain plant species, this compound may be used in toxicology studies to understand its effects on human health and the environment, as well as to develop methods for its detection and quantification in biological samples.
Used in Drug Delivery Systems:
Similar to gallotannin, 5,7,8,14-Tetrahydro-3,4,10,11-tetramethoxy-6-methyldibenz[c,g]azecin-13(6H)-one could potentially be used in drug delivery systems to improve the bioavailability and therapeutic outcomes of other pharmaceutical compounds. Further research would be needed to explore this application.
References
Boit, Flentje., Naturwiss., 47, 180 (1960)Preininger et aZ., PZanta Med., 10, 124 (1962)Mass spectrum:
Cross et aZ., Collect. Czech. Chern. Cornrnun., 30, 1335 (1965)Synthesis:
Haworth, Koepfli, Perkin., 1. Chern. Soc., 2261 (1927)Giacopello, Deulofeu., Tetrahedron Lett., 2859 (1966)
Check Digit Verification of cas no
The CAS Registry Mumber 2292-20-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2292-20:
(6*2)+(5*2)+(4*9)+(3*2)+(2*2)+(1*0)=68
68 % 10 = 8
So 2292-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO5/c1-23-9-8-15-11-20(26-3)21(27-4)12-16(15)18(24)10-14-6-7-19(25-2)22(28-5)17(14)13-23/h6-7,11-12H,8-10,13H2,1-5H3
