32113-04-5 Usage
Description
1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium, also known as Methylquinolium, is a heterocyclic chemical compound characterized by a molecular formula of C11H11N2. It features a quinolinium ring and a triaza-dien-ium functional group, which contribute to its unique properties and applications in various scientific and industrial fields.
Uses
Used in Fluorescent Dyes:
1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium is used as a fluorescent dye in the application of biological assays and imaging techniques. Its fluorescent properties allow for the visualization and tracking of biological processes, making it a valuable tool in research and diagnostics.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium serves as a precursor for the synthesis of other organic compounds. Its unique structure facilitates the creation of new molecules with potential applications in various industries, including pharmaceuticals and materials science.
Used in Antitumor and Antimicrobial Applications:
1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium has been studied for its potential antitumor and antimicrobial properties. It is used as a compound with therapeutic potential in the application of cancer treatment and infection control. Further research is needed to fully understand its efficacy and safety in these applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium is used as a compound with potential therapeutic applications. Its antitumor and antimicrobial properties make it a candidate for the development of new drugs targeting cancer and infectious diseases.
Used in Material Science:
1-(2-methylquinolin-4-yl)triaza-1,2-dien-2-ium is also used in material science as a component in the development of new materials with specific properties. Its unique structure and functional groups can contribute to the creation of advanced materials for various applications, such as sensors, catalysts, or advanced coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 32113-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32113-04:
(7*3)+(6*2)+(5*1)+(4*1)+(3*3)+(2*0)+(1*4)=55
55 % 10 = 5
So 32113-04-5 is a valid CAS Registry Number.
32113-04-5Relevant articles and documents
Efficient synthesis of 1,4-disubstituted triazolyl N-carboxamides via a simple and convenient MCR using basic alumina as solid support
Pal, Rammyani,Sarkar, Swarbhanu,Chatterjee, Nivedita,Sen, Asish Kumar
, p. 5642 - 5646 (2013/09/23)
A microwave assisted green protocol for the synthesis of 1,4-disubstituted triazolyl N-carboxamides was explored using basic alumina as solid support. The method allows domino Ullmann-type reaction, Click reaction and formation of ester or amide linkages in a single reaction vessel using Cu(phen)(PPh 3)Br and CMPA as catalyst and basic alumina as solid support in high yield. The protocol did not require addition of any external ligands or base. The method was also found to be equally good for the synthesis of bis triazole adducts.
Studies on Diazepines. XXVII. Syntheses of fully Unsaturated 1H- and 3H-1,4-benzodiazepines from 4-Quinolyl Azides
Sashida, Haruki,Fujii, Akira,Tsuchiya, Takashi
, p. 3182 - 3189 (2007/10/02)
Irradiation of the 4-azidoquinolines (7a-d) in a 1:1 mixture of methanol and dioxane containing sodium methoxide resulted in ring expansion to form the unstable fully unsaturated 1H-1,4-benzodiazepines (9a-d), which were tautomerized to the stable 3H-1,4-
