3517-61-1 Usage
Uses
Used in Pharmaceutical Synthesis:
6-hydroxy-1H-quinolin-4-one is utilized as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and biological activities, including its antioxidant, antiviral, and antitumor properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 6-hydroxy-1H-quinolin-4-one is employed as a key component in the development of new agrochemicals, leveraging its potential to combat viral infections and promote plant health.
Used in Organic Synthesis:
6-hydroxy-1H-quinolin-4-one is used as a precursor in organic synthesis for the preparation of other functionalized quinolin-4-one derivatives, which can have a range of applications in various chemical and material science fields.
Used in Medicinal Chemistry Research:
As a compound with demonstrated antioxidant, antiviral, and antitumor activities, 6-hydroxy-1H-quinolin-4-one is used in medicinal chemistry research to explore its potential in the development of new therapeutic agents and treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 3517-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3517-61:
(6*3)+(5*5)+(4*1)+(3*7)+(2*6)+(1*1)=81
81 % 10 = 1
So 3517-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-6-1-2-8-7(5-6)9(12)3-4-10-8/h1-5,11H,(H,10,12)
3517-61-1Relevant academic research and scientific papers
Reactive Nitrogenous Molecules from Meldrum's Acid Derivatives, Pyrrole-2,3-diones, and Isoxazolones
Briehl, Horst,Lukosch, Adelheid,Wentrup, Curt
, p. 2772 - 2779 (2007/10/02)
Flash vacuum pyrolysis of 5-(aminomethylidene)-2,2-dimethyl-1,3-dioxane-4,6-diones (Meldrum's acid derivatives) 12 gives 4-hydroxyquinolines/4-quinolones 15 or 3-enaminoacroleins 22 in good to excellent yields.Intermediate (aminomethylene)ketenes and imidoylketenes are directly observed and their transformation into product 22 monitored by low-temperature IR spectroscopy.Imidoylketenes are also formed and observed upon thermal CO extrusion from pyrrole-2,3-diones 16.Isocyanoamines and fulminates are generated by pyrolysis of hydrazono- or oximino-Meldrum's acid derivatives 32 and 39, monitored by IR spectroscopy, and found to rearrange to cyanamides and cyanates, depending on substituents.The thermal reactions of isoxazol-5(4H)-ones and Meldrum's acid derivatives are compared and discussed.
