23443-05-2 Usage
Uses
Used in Pharmaceutical Industry:
5-Chloroquinolin-4-ol is used as an intermediate in the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties. It serves as a key building block in the development of new drugs, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical industry, 5-chloroquinolin-4-ol is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its antimicrobial and antifungal properties make it a valuable component in the development of effective solutions for crop protection and disease control.
Used in Antimicrobial Applications:
5-Chloroquinolin-4-ol is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, including bacteria and fungi. This property makes it suitable for use in applications where controlling microbial growth is essential, such as in the preservation of food products or in the development of antimicrobial coatings and surfaces.
Used in Antifungal Applications:
Leveraging its antifungal properties, 5-chloroquinolin-4-ol is employed in antifungal applications to combat fungal infections and prevent the growth of fungi in various settings. This can be particularly useful in agricultural, medical, and industrial contexts where fungal contamination can pose risks to health or product quality.
Check Digit Verification of cas no
The CAS Registry Mumber 23443-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,4 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23443-05:
(7*2)+(6*3)+(5*4)+(4*4)+(3*3)+(2*0)+(1*5)=82
82 % 10 = 2
So 23443-05-2 is a valid CAS Registry Number.
23443-05-2Relevant academic research and scientific papers
Synthesis of ring-substituted 4-aminoquinolines and evaluation of their antimalarial activities
Madrid, Peter B.,Sherrill, John,Liou, Ally P.,Weisman, Jennifer L.,DeRisi, Joseph L.,Guy, R. Kiplin
, p. 1015 - 1018 (2007/10/03)
A simple two-step synthesis method was used to make 51 B-ring-substituted 4-hydroxyquinolines allowing analysis of the effect of ring substitutions on inhibition of growth of chloroquine sensitive and resistant strains of Plasmodium falciparum, the dominant cause of malaria morbidity. Substituted quinoline rings other than the 7-chloroquinoline ring found in chloroquine were found to have significant activity against the drug-resistant strain of P. falciparum W2.
