1218-51-5 Usage
Uses
1. Used in Pharmaceutical Applications:
(7R)-1,3,4,7,7aα,8,9,10,11,13,14,14aα-Dodecahydro-7α,14α-methano-2H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-6-one may be utilized as an active pharmaceutical ingredient or a key intermediate in the synthesis of various drugs due to its unique structure and potential biological activities.
2. Used in Chemical Synthesis:
As a complex organic compound, (7R)-1,3,4,7,7aα,8,9,10,11,13,14,14aα-Dodecahydro-7α,14α-methano-2H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-6-one could serve as a building block or a starting material for the synthesis of other complex molecules, including novel pharmaceuticals, agrochemicals, or specialty chemicals.
3. Used in Research and Development:
(7R)-1,3,4,7,7aα,8,9,10,11,13,14,14aα-Dodecahydro-7α,14α-methano-2H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-6-one's unique structure and stereochemistry make it an interesting candidate for research in various scientific fields, such as medicinal chemistry, organic synthesis, and materials science. It could be used to study the effects of stereochemistry on biological activity, to develop new synthetic methods, or to explore its potential as a component in advanced materials.
4. Used in Drug Delivery Systems:
Similar to other complex organic compounds, (7R)-1,3,4,7,7aα,8,9,10,11,13,14,14aα-Dodecahydro-7α,14α-methano-2H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-6-one may be investigated for its potential use in drug delivery systems, where it could be employed as a carrier, enhancer, or modifier to improve the delivery, bioavailability, and therapeutic outcomes of various drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 1218-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1218-51:
(6*1)+(5*2)+(4*1)+(3*8)+(2*5)+(1*1)=55
55 % 10 = 5
So 1218-51-5 is a valid CAS Registry Number.
1218-51-5Relevant academic research and scientific papers
Visible-Light-Mediated Efficient Metal-Free Catalyst for α-Oxygenation of Tertiary Amines to Amides
Zhang, Yu,Riemer, Daniel,Schilling, Waldemar,Kollmann, Jiri,Das, Shoubhik
, p. 6659 - 6664 (2018/06/25)
A metal-free system has been discovered for the efficient α-oxygenation of tertiary amines to the corresponding amides using oxygen as an oxidant. This visible-light-mediated oxygenation reaction exhibited excellent substrates scope under mild reaction conditions and generated water as the only byproduct. The synthetic utility of this approach has been demonstrated by applying onto drug molecules. At the end, detailed mechanistic reactions clearly showed the role of oxygen and the photocatalyst.
III. Thioanalogs of sparteine lactams. (+)-17-Thionosparteine and its perchlorate salt
Wysocka, Waleria,Kolano?, Renata,Borowiak, Teresa,Dutkiewicz, Grzegorz
, p. 563 - 570 (2007/10/03)
(+)-17-Thionosparteine and its perchlorate have been obtained and characterized by IR and NMR-spectroscopy as well as by X-ray diffraction analysis. Introduction of the thiolactam group into the cis-quinolizidine system causes conformational rigidity of t
Lactams of sparteine
Golebiewski, W. Marek,Spenser, Ian D.
, p. 716 - 719 (2007/10/02)
(2,2-2H2)Sparteine, (6-2H)sparteine, (10,10-2H2)sparteine, (15,15-2H2)sparteine, (17α-2H)sparteine, (17β-2H)sparteine, (17,17-2H2)sparteine, (17α-2H)lupanine, and (17β-2H)lupanine were prepared and employed to assign the 1H nmr spectrum of sparteine.Contrary to a published report, photochemical oxidation of sparteine does not lead to 15-oxosparteine but to 17-oxosparteine.
