50741-46-3 Usage
Description
QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER, also known as Ethyl 3-quinolinecarboxylate, is an organic compound derived from quinolinecarboxylic acid. It is prepared through a chemical process involving thionyl chloride and esterification with ethanol. QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER has unique photochemical properties, with its reactions in various alcohols and cyclohexane being influenced by the nature of the solvent.
Uses
Used in Pharmaceutical Industry:
QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a starting material for the synthesis of various pharmaceutical compounds, such as 5-quinolinemethanol and ethyl 3-quinolineacetate. These synthesized compounds have potential applications in the development of drugs targeting different medical conditions.
Used in Chemical Research:
In the field of chemical research, QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER serves as a valuable compound for studying its photochemical reactions in different solvents. Understanding these reactions can provide insights into the compound's properties and potential applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 50741-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,4 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50741-46:
(7*5)+(6*0)+(5*7)+(4*4)+(3*1)+(2*4)+(1*6)=103
103 % 10 = 3
So 50741-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c1-2-15-12(14)10-7-9-5-3-4-6-11(9)13-8-10/h3-8H,2H2,1H3
50741-46-3Relevant articles and documents
-
Blicke,Gearien
, p. 3587 (1954)
-
NMR studies of new heterocycles tethered to purine moieties with anticancer activity
Fernández-Sáez, Nerea,Campos, Joaquín M.,Camacho, María Encarnación,Carrión, María Dora
, p. 331 - 341 (2019/04/30)
-
Polythiophene-Encapsulated Bimetallic Au-Fe3O4 Nano-Hybrid Materials: A Potential Tandem Photocatalytic System for Nondirected C(sp2)-H Activation for the Synthesis of Quinoline Carboxylates
Kaur, Mandeep,Pramanik, Subhamay,Kumar, Manoj,Bhalla, Vandana
, p. 2007 - 2021 (2017/08/17)
Hetero-oligophenylene derivative 3 appended with thiophene moieties has been designed and synthesized which undergoes aggregation to form J-type fluorescent aggregates in in H2O/THF (7/3) media. These aggregates served as reactors for the preparation of bimetallic Au-Fe3O4 NPs. During the reduction process, aggregates of derivative 3 were oxidized to the polythiophene species 4. Interestingly, the polythiophene species 4, having a fibrous morphology, served as a shape- and morphology-directed template for assembly of bimetallic Au-Fe3O4 NPs in a flower-like arrangement. Furthermore, polythiophene-encapsulated bimetallic 4:Au-Fe3O4 nanohybrid materials served as an efficient and recyclable catalytic system for C(sp2)-H bond activation of unprotected electron-rich anilines for the construction of synthetically versatile quinoline carboxylates via C-H activation, carbonylation, and subsequent annulation under mild and eco-friendly conditions (aqueous media, room temperature, visible-light irradiation, and aerial conditions).
