1450997-93-9 Usage
Uses
Used in Pharmaceutical Applications:
(E)-4-(4-chlorobenzylidene)-11-(4-chlorophenyl)-2,3,4,11-tetrahydro-1H-pyrido[2,1-b]quinazoline is used as a potential therapeutic agent for modulating specific biological pathways. Its complex structure allows it to interact with various biological systems, which may have implications for the treatment of certain medical conditions. (E)-4-(4-chlorobenzylidene)-11-(4-chlorophenyl)-2,3,4,11-tetrahydro-1H-pyrido[2,1-b]quinazoline's ability to modulate these pathways could make it a valuable tool in the development of new drugs and therapies.
Used in Research and Development:
In the field of medicinal chemistry, (E)-4-(4-chlorobenzylidene)-11-(4-chlorophenyl)-2,3,4,11-tetrahydro-1H-pyrido[2,1-b]quinazoline serves as a valuable compound for research and development. Its unique structure and potential interactions with biological systems make it an interesting candidate for further study, with the aim of understanding its pharmacological properties and potential applications in drug discovery.
Used in Drug Design and Optimization:
(E)-4-(4-chlorobenzylidene)-11-(4-chlorophenyl)-2,3,4,11-tetrahydro-1H-pyrido[2,1-b]quinazoline's complex structure and potential biological activity make it a useful starting point for drug design and optimization efforts. By studying its interactions with biological targets and understanding its pharmacological profile, researchers can work to modify and improve the compound to enhance its therapeutic potential and safety profile for specific medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1450997-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,9,9 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1450997-93:
(9*1)+(8*4)+(7*5)+(6*0)+(5*9)+(4*9)+(3*7)+(2*9)+(1*3)=199
199 % 10 = 9
So 1450997-93-9 is a valid CAS Registry Number.
1450997-93-9Relevant academic research and scientific papers
Synthesis of highly substituted 4H-pyrido[1,2- A ]pyrimidines via a one-pot three-component condensation reaction
Yang, Kai,Xiang, Jinbao,Bao, Guochen,Dang, Qun,Bai, Xu
supporting information, p. 519 - 524 (2013/09/24)
A one-pot three-component reaction, involving condensation of 2-aminopyridines, aldehydes, and ketones/aldehydes under trifluoromethanesulfonic acid catalysis, provides rapid access to highly substituted novel 4H-pyrido[1,2-a]pyrimidines.
