38366-04-0 Usage
Uses
Used in Pharmaceutical Industry:
4,5,6,9-Tetramethoxyindeno[1,2,3-ij]isoquinoline is used as a pharmaceutical candidate for its potential therapeutic applications. Its unique chemical structure allows it to interact with various biological targets, making it a promising compound for the development of new drugs.
Used in Chemical Research:
4,5,6,9-Tetramethoxyindeno[1,2,3-ij]isoquinoline is also used as a research tool in the field of organic chemistry and drug discovery. Its unique structure and properties make it an interesting subject for studying the synthesis, reactivity, and potential applications of isoquinoline alkaloids.
Used in Drug Delivery Systems:
Similar to gallotannin, 4,5,6,9-Tetramethoxyindeno[1,2,3-ij]isoquinoline can be employed in the development of novel drug delivery systems. Its chemical properties may allow for the design of targeted drug delivery systems, improving the bioavailability and therapeutic outcomes of various pharmaceutical agents.
References
Cava et al., Tetrahedron, 31, 1667 (1975)
Check Digit Verification of cas no
The CAS Registry Mumber 38366-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,6 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38366-04:
(7*3)+(6*8)+(5*3)+(4*6)+(3*6)+(2*0)+(1*4)=130
130 % 10 = 0
So 38366-04-0 is a valid CAS Registry Number.
38366-04-0Relevant academic research and scientific papers
A route to azafluoranthene natural products through direct arylation
Ponnala, Shashikanth,Harding, Wayne W.
, p. 1107 - 1115 (2013/04/10)
Microwave-assisted direct arylation reactions were successfully employed in the synthesis of azafluoranthene alkaloids for the first time. Direct arylation reactions on a diverse set of phenyltetrahydroisoquinolines produces the indeno[1,2,3-ij]isoquinoli
Total Syntheses of Azafluoranthene Alkaloids: Rufescine and Imeluteine
Boger, Dale L.,Brotherton, Christine E.
, p. 4050 - 4055 (2007/10/02)
Total syntheses of rufescine and imeluteine, azafluoranthene alkaloids isolated from Abuta imene and Abuta rufescens, are detailed and are based on the utilization of the inverse electron demand Diels-Alder reactions of 3-carbomethoxy-2-pyrones for the selective and controlled introduction of oxygenated aromatics.
