71082-47-8 Usage
General Description
6-Methoxy-3-quinolinecarboxylic acid is a chemical compound that belongs to the quinolinecarboxylic acid family. It is also known as 6-Methyl-3-methoxyquinoline-4-carboxylic acid or 3-Carboxy-6-methoxyquinoline. 6-Methoxy-3- quinolinecarboxvlic acid is a derivative of quinoline and is often used in the synthesis of pharmaceuticals and agrochemicals. It has potential biological activity and is being studied for its potential therapeutic applications, particularly in the treatment of cancer and infectious diseases. 6-Methoxy-3-quinolinecarboxylic acid is also used as a building block in organic synthesis and as a research tool in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 71082-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,8 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71082-47:
(7*7)+(6*1)+(5*0)+(4*8)+(3*2)+(2*4)+(1*7)=108
108 % 10 = 8
So 71082-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c1-15-9-2-3-10-7(5-9)4-8(6-12-10)11(13)14/h2-6H,1H3,(H,13,14)
71082-47-8Relevant articles and documents
Initial Route Scouting and Final Process Development for the Multi-Kg Production of 3-Fluoro-6-methoxyquinoline from p-Anisidine and 2-Fluoromalonic Acid
Sch?fer, Gabriel,Fleischer, Tony,Blumer, Nicole,Udry, Megan,Reber, Stefan,Stansfield, Ian,Liu, Yuanhua,Li, Yan,Li, Pixu
supporting information, p. 347 - 357 (2022/02/01)
A scalable route to 3-fluoro-6-methoxyquinoline needed to be developed as multi-kg amounts of this heterocycle were required. Initial route development focused on the formation of the key C-F bond via a Balz-Schiemann reaction or electrophilic fluorinatio
Syntheses and Reactions of Diazepinoquinolines
Guendel, Wolf-H.,Bohnert, Sabine
, p. 769 - 777 (2007/10/02)
Three routes for the preparation of diazepinoquinolines (1) have been studied.The best yields resulted by starting from the amides of N-(3-quinolylcarbonyl)-N-alkyl-amino acids (5).Quaternization to 9, intramolecular cyclization under the influence of base to 10, oxidation to 11 and debenzylation by catalytic hydrogenation gave 1. - Keywords: Quinolinium Salts, Cyclization Reaction