83508-83-2 Usage
Uses
Used in Pharmaceutical Industry:
Methyl (41S,12R,13aR)-13a-ethyl-12-hydroxy-2,3,41,5,6,12,13,13aoctahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate is used as a nootropic agent for combating the effects of aging or in conjunction with other nootropics for a variety of purposes. It acts as a peripheral vasodilator, increasing blood flow to the brain, which can help improve cognitive function and memory.
Used in Drug Delivery Systems:
methyl (41S,12R,13aR)-13a-ethyl-12-
hydroxy-2,3,41,5,6,12,13,13aoctahydro-
1H-indolo[3,2,1-
de]pyrido[3,2,1-ij][1,5]naphthyridine-
12-carboxylate can be employed in drug delivery systems to enhance the bioavailability and therapeutic outcomes of various drugs. Its unique molecular structure allows for the development of novel drug delivery systems, such as organic and metallic nanoparticles, which can improve the delivery and efficacy of the compound in treating specific conditions.
Used in Chemical Research:
Methyl (41S,12R,13aR)-13a-ethyl-12-hydroxy-2,3,41,5,6,12,13,13aoctahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate can be used as a research tool in chemical and pharmaceutical research. Its unique properties and structure make it a valuable compound for studying various chemical reactions and mechanisms, as well as for the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 83508-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83508-83:
(7*8)+(6*3)+(5*5)+(4*0)+(3*8)+(2*8)+(1*3)=142
142 % 10 = 2
So 83508-83-2 is a valid CAS Registry Number.
83508-83-2Relevant academic research and scientific papers
Synthesis of 18-hydroxyvincamines and epoxy-1,14-secovincamines; A new proof for the aspidospermane-eburnane rearrangement
Nemes, Andras,Szantay Jr., Csaba,Czibula, Laszlo,Greiner, Istvan
, p. 2347 - 2362 (2008/09/18)
Chemical transformations started from tabersonine were studied. A one-pot oxidative ring-transformation with permaleic acid in methanol yielded 17,18-dehydrovincamine. Hydroboration-oxidation of the latter compound led to alkaloid 17,18-dehydrovincamone. Hydroboration-oxidation of tabersonine resulted 14β-hydroxyvincadifformine and 15β-hydroxyvincadifformine. Allowing 14β- and 15β- hydroxyvincadifformines to react with permaleic acid/methanol provided 1,14-secovincamines, serving as new evidence for the mechanism of the aspidospermane-eburnane transformation. On the other hand 18β-hydroxyvincamine was obtained from 14β-hydroxyvincadifformine by reaction with 3-chloroperbenzoic acid and successive treatment with triphenylphosphine/aqueous acetic acid.
