13233-45-9 Usage
Uses
Used in Pharmaceutical Industry:
1,2,3,4,6,7,12,12b-Octahydro-12-methylindolo[2,3-a]quinolizine is used as a pharmaceutical compound for its potential therapeutic properties. The compound's structure and alkaloid nature suggest that it may have various biological activities, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
1,2,3,4,6,7,12,12b-Octahydro-12-methylindolo[2,3-a]quinolizine is used as a research compound in the field of chemistry. Its unique structure and properties make it an interesting subject for studying the chemical properties of quinolizine alkaloids and their potential applications in various industries.
Used in Agricultural Industry:
1,2,3,4,6,7,12,12b-Octahydro-12-methylindolo[2,3-a]quinolizine, being a natural compound found in cranberries, may have potential applications in the agricultural industry. It could be used for enhancing the nutritional value of cranberries or for developing new cranberry-based products with potential health benefits.
References
Jankowski, Godin, Cundasawmy, Can. J. Chern., 52,2064 (1974)
Check Digit Verification of cas no
The CAS Registry Mumber 13233-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13233-45:
(7*1)+(6*3)+(5*2)+(4*3)+(3*3)+(2*4)+(1*5)=69
69 % 10 = 9
So 13233-45-9 is a valid CAS Registry Number.
13233-45-9Relevant academic research and scientific papers
One-pot tandem route to fused indolizidines and quinolizidines: Application in the synthesis of alkaloids and bioactive compounds
Song, Qiao,Liu, Yan,Cai, Linlin,Cao, Xinyu,Qian, Shan,Wang, Zhouyu
, p. 1713 - 1716 (2021/03/08)
Fused indolizidines and quinolizidines are important skeletons in a variety of natural products and pharmacologically important compounds. A one-pot tandem route from amide to fused indolizidines and quinolizidines is disclosed. This method is conducted in mild conditions and shows well tolerance of functional groups. It is also easy to be scaled up to gram scale and can be applied smoothly to the total synthesis of alkaloids such as (±)-crispine A, (±)-xylopinine, (±)-desbromoarborescidine A, (±)-harmicine and other bioactive substances.
Synthetic method of tetrahydroisoquino ring compound and tetrahydro-beta-carbo ring compound
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Paragraph 0047-0052; 0163; 0165-0167, (2020/12/09)
The invention provides a synthetic method of a tetrahydroisoquino ring compound and a tetrahydro-beta-carbo ring compound, and belongs to the technical field of synthesis. According to the method forsynthesizing the tetrahydroisoquino and the tetrahydro-b
