79082-02-3 Usage
Uses
Used in Pharmaceutical Industry:
(6R,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline is used as a potential pharmaceutical candidate for various applications due to its unique structure and potential biological activity. Its complex molecular composition and the presence of methoxy and methyl groups, along with the dioxolo ring system, may contribute to its pharmacological properties, making it a promising compound for further research and development in the pharmaceutical field.
Used in Medicinal Research:
In the field of medicinal research, (6R,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline is used as a compound of interest for exploring its potential therapeutic applications. (6R,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline's unique structure and the presence of various functional groups may provide insights into its interactions with biological targets, potentially leading to the development of new drugs or therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 79082-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,8 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79082-02:
(7*7)+(6*9)+(5*0)+(4*8)+(3*2)+(2*0)+(1*2)=143
143 % 10 = 3
So 79082-02-3 is a valid CAS Registry Number.
79082-02-3Relevant academic research and scientific papers
Studies in Protoberberine Alkaloids: Part XIX - Synthesis of (+/-)-Thalictrifoline, (+/-)-Sinactine and (+/-)-Cavidine
Pai, B. R.,Natarajan, S.,Suguna, H.,Rajeswari, S.,Chandrasekaran, S.,Nagarajan, K.
, p. 607 - 611 (2007/10/02)
(+/-)-Thalictrifoline (14), (+/-)-sinactine (13) and (+/-)-cavidine (18) have been synthesised from trans- and cis-13-carboxy-9,10-methylenedioxy-2,3-dimethoxy-8-oxo-tetrahydroprotoberberines (8 and 9). 8 and 9 are obtained by condensing 3,4-methylenedioxyhomophthalic anhydride (6) and 6,7-dimethoxyisoquinoline (7).
Absolute Configurations of the cis- and trans-13-Methyltetrahydroprotoberberines. Total Synthesis of (+)-Thalictricavine, (+)-Canadine, (+/-)-, (-)-, and (+)-Thalictrifoline, and (+/-)-, (-)-, and (+)-Cavidine
Iwasa, Kinuko,Gupta, Yash Pal,Cushman, Mark
, p. 4744 - 4750 (2007/10/02)
The tetrahydroprotoberberine alkaloids (+)-thalictricavine and (+)-canadine have been synthesized from an optically resolved (+)-13-carboxy-7,8,13,14-tetrahydro-9-oxoprotoberberine .This establishes the absolute configuration of (+)-thalictricavine as 13S,14R. (+)-Thalictrifoline and (+)-cavidine have also been prepared from a common intermediate, (+)-32, whose absolute configuration was established by correlation with (+)-26.This determines the absolute configuration of (+)-thalictrifoline as 13R,14R, of (+)-corydalic acid methyl ester (22) as 3R,4R, and of the protopine (+)-corycavine (20) as 13R.
