100517-42-8 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-Chloro-2-hydroxyquinoline-3-carbaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its biological activities, which include antibacterial, antifungal, and anticancer properties. Its presence in these industries aids in the development of new drugs and pesticides for treating diseases and controlling pests, respectively.
Used in Anticancer Research:
In the field of oncology, 4-Chloro-2-hydroxyquinoline-3-carbaldehyde is used as a potential anticancer agent. It has been studied for its ability to target and combat cancer cells, making it a valuable compound in the search for novel therapeutics to treat various types of cancer.
Used in Metal Ion Detection:
4-Chloro-2-hydroxyquinoline-3-carbaldehyde also serves as a fluorescent probe for the detection of metal ions. Its application in this area is crucial for environmental monitoring and analytical chemistry, where the sensitive and selective detection of metal ions is required.
Used in Organic Synthesis as a Reagent:
Furthermore, 4-Chloro-2-hydroxyquinoline-3-carbaldehyde is utilized as a reagent in organic synthesis. Its unique structure and functional groups make it a versatile component in the creation of complex organic molecules, contributing to the advancement of organic chemistry and the development of new chemical compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 100517-42-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,1 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100517-42:
(8*1)+(7*0)+(6*0)+(5*5)+(4*1)+(3*7)+(2*4)+(1*2)=68
68 % 10 = 8
So 100517-42-8 is a valid CAS Registry Number.
100517-42-8Relevant academic research and scientific papers
A convenient synthesis of 8,9,10,11-tetrahydrodibenzo[b,h] [1,6]naphthyridin-6(5H)ones
Arul Prakash,Rajendran
, p. 353 - 358 (2007/10/03)
Substituted 8,9,10,11-tetrahydrodibenzo[b,h][1,6]naphthyridin-6(5H)ones (5) have been synthesized by the condensation of 4-amino-3-formylquinolin-2(1H)ones (4) with cyclohexanone in presence of acetic acid and sulphuric acid. The precusors have been obtained by the animation of 4-chloro-3-formylquinolin-2(1H)ones (3).
