17326-31-7 Usage
Derivative of pyrido[1,2-a]pyrimidin-4-one
Heterocyclic compound with potential biological activity
Contains a morpholine ring
A five-membered ring containing four carbon atoms and one nitrogen atom
Contains a pyrido[1,2-a]pyrimidin-4-one core structure
A central structure that contributes to the compound's potential pharmacological activity
Potential pharmacophore
A compound that can be used as a starting point for drug design due to its potential biological activity
Limited documentation of chemical properties
The specific chemical properties of 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one have not been widely studied
Limited documentation of pharmacological activities
The pharmacological activities of 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one have not been widely studied
Potential for pharmaceutical research and development
Due to its unique structure and potential biological activity, 2-(morpholin-4-yl)-4H-pyrido[1,2-a]pyrimidin-4-one holds promise for further research and development in the field of pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 17326-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,2 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17326-31:
(7*1)+(6*7)+(5*3)+(4*2)+(3*6)+(2*3)+(1*1)=97
97 % 10 = 7
So 17326-31-7 is a valid CAS Registry Number.
17326-31-7Relevant academic research and scientific papers
Generation of functionalized azomethine ylides and their application to stereoselective heterocycle synthesis: an equivalent process of C-unsubstituted nitrile ylide cycloaddition reaction
Kawashima, Keisuke,Kakehi, Akikazu,Noguchi, Michihiko
, p. 1630 - 1643 (2007/10/03)
The synthetic process equivalent to C-unsubstituted (CH) nitrile ylides cycloaddition reaction is achieved via cycloaddition of NH-azomethine ylide and the following fission reaction of the cycloadducts under acidic conditions. Cycloaddition of NH-azometh
RICERCHE SU DERIVATI PIRIDOPIRIMIDINICI. Nota I - Sintesi di 4-(dialchilammino)-2H-piridopirimidin-2-oni.
Roma, G.,Ermili, A.,Braccio, M. Di,Mazzei, M.
, p. 747 - 758 (2007/10/02)
Reaction of the N,N-dialkylethoxycarbonylacetamide-POCl3 reactant with 2-aminopyridine in refluxing dichloroethane yielded 4-(dialkylamino)-2H-pyridopyrimidine-2-ones (IV) together with generally lower quantities of isomeric 2-(dialkylamino)-4H-pyridopyrimidin-4-ones (V).Some compounds (V) were obtained also by reaction of 2-chloro-4H-pyridopyrimidin-4-one (VI) with the suitable amine in confirmation of their structure.In addition, the differences in the properties and in the spectroscopic characteristics of the two classes of isomers are reported.
