3382-84-1 Usage
Uses
Used in Pharmaceutical Research and Development:
(11aR)-3-but-3-en-1-yldecahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one is used as a research compound for exploring its potential applications in drug discovery and medicinal chemistry. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Drug Discovery:
In the field of drug discovery, (11aR)-3-but-3-en-1-yldecahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one is used as a starting point for designing and synthesizing new pharmaceutical compounds. Its complex molecular structure may offer novel interactions with biological targets, leading to the development of innovative treatments for various diseases.
Used in Medicinal Chemistry:
(11aR)-3-but-3-en-1-yldecahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one is employed in medicinal chemistry as a structural template for the modification and optimization of drug candidates. Its diazocin ring system and butenyl side chain can be modified to enhance the compound's pharmacological properties, such as potency, selectivity, and bioavailability.
Note: Since the provided materials do not specify any particular application industry or reason for the use of (11aR)-3-but-3-en-1-yldecahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one, the uses listed above are general applications based on its role as a chemical compound in pharmaceutical research and development. Further information would be required to provide more specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3382-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3382-84:
(6*3)+(5*3)+(4*8)+(3*2)+(2*8)+(1*4)=91
91 % 10 = 1
So 3382-84-1 is a valid CAS Registry Number.
3382-84-1Relevant academic research and scientific papers
The Enantioselective Total Synthesis of Bisquinolizidine Alkaloids: A Modular “Inside-Out” Approach
Scharnagel, Dagmar,Goller, Jessica,Deibl, Nicklas,Milius, Wolfgang,Breuning, Matthias
, p. 2432 - 2435 (2018/02/16)
Bisquinolizidine alkaloids are characterized by a chiral bispidine core (3,7-diazabicyclo[3.3.1]nonane) to which combinations of an α,N-fused 2-pyridone, an endo- or exo-α,N-annulated piperidin(on)e, and an exo-allyl substituent are attached. We developed a modular “inside-out” approach that permits access to most members of this class. Its applicability was proven in the asymmetric synthesis of 21 natural bisquinolizidine alkaloids, among them more than ten first enantioselective total syntheses. Key steps are the first successful preparation of both enantiomers of C2-symmetric 2,6-dioxobispidine by desymmetrization of a 2,4,6,8-tetraoxo precursor, the construction of the α,N-fused 2-pyridone by using an enamine-bromoacrylic acid strategy, and the installation of endo- or, optionally, exo-annulated piperidin(on)es.
