529-79-3 Usage
Uses
Used in Pharmaceutical Research:
(5S,11S)-5,6,11,12-Tetrahydro-2,3,8,9-tetramethoxy-5,11-epiminodibenzo[a,e]cyclooctene is used as a research compound for its potential applications in drug discovery and development. Its unique structure and chirality make it a promising candidate for further exploration in the pharmaceutical industry.
Used in Chemical Research:
(5S,11S)-5,6,11,12-Tetrahydro-2,3,8,9-tetramethoxy-5,11-epiminodibenzo[a,e]cyclooctene is used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique substitution pattern and cycloalkene nature offer opportunities for further chemical research and development.
Used in Drug Delivery Systems:
In the field of drug delivery, (5S,11S)-5,6,11,12-Tetrahydro-2,3,8,9-tetramethoxy-5,11-epiminodibenzo[a,e]cyclooctene could be used as a component in the design of novel drug delivery systems. Its structural features may allow for the development of targeted or controlled-release drug formulations, enhancing the efficacy and bioavailability of therapeutic agents.
Used in Material Science:
(5S,11S)-5,6,11,12-Tetrahydro-2,3,8,9-tetramethoxy-5,11-epiminodibenzo[a,e]cyclooctene may also find applications in material science, where its unique structural properties could be exploited to create new materials with specific characteristics, such as improved stability or novel optical, electronic, or mechanical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 529-79-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 529-79:
(5*5)+(4*2)+(3*9)+(2*7)+(1*9)=83
83 % 10 = 3
So 529-79-3 is a valid CAS Registry Number.
529-79-3Relevant academic research and scientific papers
An Enantioselective Access to 1-Alkyl-1,2,3,4-tetrahydroisoquinolines. Application to a New Synthesis of (-)-Argemonine
Youte, Jean-Jacques,Barbier, Denis,Al-Mourabit, Ali,Gnecco, Dino,Marazano, Christian
, p. 2737 - 2740 (2007/10/03)
Potassium ferricyanide oxidation of salt 1 gave isoquinolinone 7 whose treatment with Grignard reagents resulted in a high-yield formation of substituted isoquinolinium salts 5. The selectivity of the reduction of these salts to give derivatives 6 has been studied. Particularly good selectivities (82-84%) were observed when R is a benzylic group. On the basis of these results, a practical and enantioselective synthesis of the natural alkaloid (-)-argemonine is presented.
A novel asymmetric route to the 1,3-disubstituted tetrahydroisoquinoline, (-)-argemonine
Munchhof, Michael J.,Meyers
, p. 4607 - 4610 (2007/10/03)
Chiral bicyclic lactam 13 was converted to the natural product (-)-argemonine 9 in six steps. This novel route to argemonine represents a general strategy for the preparation of chiral 1,3-disubstituted tetrahydroisoquinolines.
