41493-46-3 Usage
Description
[1,2,4]triazolo[4,3-a]quinolin-1(2H)-one is a complex heterocyclic chemical compound with a triazoloquinolinone backbone. It belongs to a class of organic compounds that contain at least one atom other than carbon in the ring structure. [1,2,4]triazolo[4,3-a]quinolin-1(2H)-one has garnered interest in the field of medicinal chemistry due to its potential as a pharmacophore for drug design, with its unique structure and potential bioactivity making it a promising target for further research into pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
[1,2,4]triazolo[4,3-a]quinolin-1(2H)-one is used as a pharmacophore for drug design in the pharmaceutical industry. Its unique structure and potential bioactivity make it a valuable candidate for the development of new drugs with various therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [1,2,4]triazolo[4,3-a]quinolin-1(2H)-one is used as a research target to explore its potential biological activities and therapeutic properties. [1,2,4]triazolo[4,3-a]quinolin-1(2H)-one's triazoloquinolinone backbone offers opportunities for the discovery of novel drug candidates with diverse applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 41493-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,9 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41493-46:
(7*4)+(6*1)+(5*4)+(4*9)+(3*3)+(2*4)+(1*6)=113
113 % 10 = 3
So 41493-46-3 is a valid CAS Registry Number.
41493-46-3Relevant articles and documents
The Base-Promoted Annulation of 2-Hydrazinyl Pyridine and CO2 toward Triazolones
Wu, Xiaopeng,Sun, Song,Wang, Bingbing,Cheng, Jiang
supporting information, p. 3855 - 3859 (2017/11/15)
A base-promoted annulation of 2-hydrazinyl pyridine and atmospheric pressure of CO2 has been developed in the presence of silane as reducing reagent, affording a series of triazolones in moderate to excellent yields. CO2 served as a carbonyl source in this transfomation. Moreover, benzamidrazones also worked well under this procedure. Thus, it represents a green, sustainable and straightforward pathway to access triazolone frameworks. (Figure presented.).
Agent for the control of plant-pathogenic organisms
-
, (2008/06/13)
Methods employing and compositions comprising, for the control of plant-pathogenic organisms, specified s-triazolo(4,3-a)quinoline compounds, some of which are claimed as novel compounds.
