1447813-90-2 Usage
Uses
Used in Medicinal Chemistry:
(5aS,10bR)-2-(2,6-dimethoxyphenyl)-4,5a,6,10b-tetrahydroindeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium chloride is used as a potential candidate in medicinal chemistry for its unique structure that may offer novel interactions with biological targets, leading to the development of new therapeutic agents.
Used in Research and Development:
In the field of research and development, (5aS,10bR)-2-(2,6-dimethoxyphenyl)-4,5a,6,10b-tetrahydroindeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium chloride is used as a research tool to study biological systems. Its complex structure and charged nitrogen atom may provide insights into various biological processes and help in understanding the mechanisms of action of similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1447813-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,8,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1447813-90:
(9*1)+(8*4)+(7*4)+(6*7)+(5*8)+(4*1)+(3*3)+(2*9)+(1*0)=182
182 % 10 = 2
So 1447813-90-2 is a valid CAS Registry Number.
1447813-90-2Relevant academic research and scientific papers
Highly enantioselective intermolecular stetter reaction of simple acrylates: Synthesis of α-chiral γ-Ketoesters
Wurz, Nathalie E.,Daniliuc, Constantin G.,Glorius, Frank
, p. 16297 - 16301 (2013/02/22)
Simple Stetter: A novel N-heterocyclic carbene (NHC) was designed by combining an electron-rich 2,6-dimethoxy substituent and an underestimated yet promising chiral motif. With this NHC in hand, a highly enantioselective intermolecular Stetter reaction of simple acrylates was developed, yielding versatile α-chiral γ-ketoesters. This represents the first catalytic asymmetric route towards these valuable compounds (see scheme).
