86814-56-4 Usage
Uses
Used in Organic Synthesis:
2-Bromo-3-hydroxyquinoline serves as a valuable building block in organic synthesis, facilitating the creation of a variety of complex organic molecules. Its unique structure allows for further functionalization and modification, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Bromo-3-hydroxyquinoline is utilized as a key intermediate in the development of new drugs. Its potential antimicrobial and anticancer properties make it a promising candidate for the discovery of novel therapeutic agents. Researchers are actively investigating its biological activity and exploring its potential as a lead compound in drug design.
Used in Antimicrobial Applications:
2-Bromo-3-hydroxyquinoline has been studied for its antimicrobial properties, demonstrating effectiveness against various types of bacteria and fungi. Its ability to disrupt microbial cell membranes and inhibit essential cellular processes makes it a potential candidate for the development of new antimicrobial agents to combat drug-resistant infections.
Used in Anticancer Applications:
2-BroMo-3-hydroxyquinoline has also been investigated for its anticancer potential, showing promise in inhibiting the growth and proliferation of cancer cells. Its mechanism of action may involve targeting specific cellular pathways and enzymes involved in cancer progression, making it a potential therapeutic agent for various types of cancer.
Used in Biological Imaging:
2-Bromo-3-hydroxyquinoline has been explored for its role as a fluorescent probe in biological imaging applications. Its fluorescent properties allow for the visualization and tracking of cellular processes, making it a valuable tool in cell biology research. It can be used to study protein-protein interactions, cellular localization, and other biological phenomena.
Check Digit Verification of cas no
The CAS Registry Mumber 86814-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,1 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86814-56:
(7*8)+(6*6)+(5*8)+(4*1)+(3*4)+(2*5)+(1*6)=164
164 % 10 = 4
So 86814-56-4 is a valid CAS Registry Number.
86814-56-4Relevant academic research and scientific papers
A new approach to 3-hydroxyquinoline-2-carboxylic acid
Riego, Estela,Bayó, Nuria,Cuevas, Carmen,Albericio, Fernando,álvarez, Mercedes
, p. 1407 - 1411 (2007/10/03)
Quinoline-2-carboxylic acid derivatives cap the N-terminal of several natural cyclic peptides with antitumoral activity. A new and convenient route for the preparation of 3-hydroxyquinoline-2-carboxylic acid is discussed. The preparation of the title compound is accomplished by a four-step procedure from 3-hydroxyquinoline via MOM protection of the hydroxyl group, followed by a 1,2-addition of methyllithium to the quinoline ring with concomitant oxidation, and, finally, a two-step oxidation procedure for the transformation of the methyl group to the carboxylic acid along with removal of the MOM group. Furthermore, different attempts to its preparation led to other interesting quinolines, such as 2-chloro-3-hydroxyquinoline-4-carboxylic acid and a protected 3,3′-dihydroxy-2,2′-biquinoline.
Bipyridyls and their use as inks
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, (2008/06/13)
Process employing bipyridyls as inks, of the general formula STR1 in which R, R' are, for example, alkyl and R1, R2, R3, R4, R5, R6 are, for example hydrogen or alkyl radicals, or R1 and R2 or R2 and R3, and/or R4 and R5 or R5 and R6 together with the pyridine ring form in isoquinoline or quinoline ring system.
