58844-03-4 Usage
Description
1-(2-bromoethyl)quinolinium, with the molecular formula C11H11BrN2, is a quaternary ammonium derivative of quinoline featuring a bromoethyl group attached to the quinoline ring. This cationic compound possesses a range of potential applications and properties in the fields of organic synthesis, pharmaceuticals, and as a precursor for the synthesis of other biologically active compounds.
Uses
Used in Pharmaceutical Applications:
1-(2-bromoethyl)quinolinium is used as a pharmaceutical compound for its potential as an anticancer agent. Studies have demonstrated its cytotoxic effects on cancer cells, making it a promising candidate for further research and development in cancer treatment.
Used in Organic Synthesis:
1-(2-bromoethyl)quinolinium is used as a synthetic building block for the creation of other biologically active compounds. Its unique structure and reactivity contribute to the development of novel molecules with potential applications in various industries.
Used in Coordination Chemistry:
1-(2-bromoethyl)quinolinium is used as a selective ligand for metal ions in coordination chemistry. Its ability to form stable complexes with metal ions can be exploited in the design of new materials and catalysts.
Used in Analytical Chemistry:
1-(2-bromoethyl)quinolinium is used as a fluorescent probe in biological and chemical analysis. Its optical properties make it a valuable tool for detecting and monitoring various chemical and biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 58844-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,4 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58844-03:
(7*5)+(6*8)+(5*8)+(4*4)+(3*4)+(2*0)+(1*3)=154
154 % 10 = 4
So 58844-03-4 is a valid CAS Registry Number.
58844-03-4Relevant articles and documents
One-pot synthesis of imidazopyridine derivatives
Parenty, Alexis D. C.,Cronin, Leroy
, p. 1479 - 1485 (2008/12/21)
Two highly efficient and general one-pot annulation reactions are described for the synthesis of imidazopyridine derivatives (IPs). The two procedures are complementary to each other: Whereas the first one allows the production of simpler IPs, the second
An unusual substitution reaction directed by an intramolecular re-arrangement
Parenty, Alexis D.C.,Smith, Louise V.,Cronin, Leroy
, p. 8410 - 8418 (2007/10/03)
Secondary amines and thiols undertake a substitution reaction on the side chain of 2-bromoethyl-pyridinium derivatives 'directed' by an intramolecular re-arrangement. Experimental investigations strongly indicate that the reaction is initiated by an alpha
3-Halo-cepham derivatives
-
, (2008/06/13)
Penicillin sulfoxides are converted to 3-halo-3-methyl-cepham-4-carboxylic acid esters and amides or the corresponding cephem derivatives by heating the penicillin sulfoxide precursor in a polyhaloalkane solvent to a temperature between 50° to about 150°C
