2721-50-8 Usage
Uses
Used in Coordination Chemistry:
2,3-dihydroxyquinolin-4(1H)-one is used as a chelating agent for its capacity to bind with metal ions, forming stable complexes. This property makes it valuable in various applications within coordination chemistry, such as the development of new metal complexes with potential uses in catalysis, materials science, and medicinal chemistry.
Used in Biological Research:
In the field of biological research, 2,3-dihydroxyquinolin-4(1H)-one is studied for its potential antioxidant and antiproliferative properties. These characteristics suggest that it may have applications in the development of therapeutic agents for various diseases and conditions.
Used in Neurodegenerative Disease Treatment:
2,3-dihydroxyquinolin-4(1H)-one has been investigated for its potential role in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its biological activities, including antioxidant properties, may contribute to neuroprotective effects that could be beneficial in managing these conditions.
Used as a Corrosion Inhibitor:
2,3-dihydroxyquinolin-4(1H)-one has also been recognized for its potential use as a corrosion inhibitor. Its ability to chelate metal ions can help prevent the corrosion of metal surfaces, making it a candidate for use in industrial applications where corrosion control is necessary.
Used in Organic Synthesis:
Furthermore, 2,3-dihydroxyquinolin-4(1H)-one serves as a building block in the synthesis of complex organic molecules. Its structural features make it a versatile component in the creation of a wide range of organic compounds for use in pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 2721-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2721-50:
(6*2)+(5*7)+(4*2)+(3*1)+(2*5)+(1*0)=68
68 % 10 = 8
So 2721-50-8 is a valid CAS Registry Number.
2721-50-8Relevant academic research and scientific papers
4-Hydroxy-2-quinolones. 37. Simple synthesis of 1-R-2-oxo-3,4-dihydroxyquinolines
Ukrainets,Taran,Sidorenko,Gorokhova
, p. 1334 - 1336 (2007/10/03)
3-Amino-1-R-2-oxo-4-hydroxyquinolines easily undergo acid hydrolysis with formation of the corresponding 1-R-2-oxo-3,4-dihydroxyquinolines. 1998 Plenum Publishing Corporation.
Glycine receptor antagonist pharmacophore
-
, (2008/06/13)
Methods of treating or preventing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, as well as treating neurodegenerative diseases including Alzheimer''s disease, amyotrophic lateral sclerosis, Huntington''s disease and Down''s syndrome, treating or preventing the adverse consequences of the hyperactivity of the excitatory amino acids, as well as treating anxiety, chronic pain, convulsions and inducing anesthesia are disclosed by administering to an animal in need of such treatment a compound which has high binding to the glycine receptor.
Ylides of Heterocycles, VIII. Reactions of Iodonium-Ylides with Acids
Pongratz, Erik,Kappe, Thomas
, p. 231 - 242 (2007/10/02)
The reaction of various organic and inorganic acids (HX) with iodonium ylides 2 leads to nucleophilic substitution of the iodobenzene substituent by the anion X(-) to yield the heterocycles 5.Some of them are hydrolyzed to the hydroxy compounds 3 or reduced to the starting compounds 1 under the reaction conditions.Reaction of the iodonium ylide 2b with monomethyl sulfate gives the salt 9, which with bases undergoes nucleophilic substitution to compounds 8 and 10-12, respectively, or is converted to 2b again. - Keywords: 3-Acetoxy-4-hydroxy-2-quinolones; 2-Oxoquinoline-4-olates; 3-Substituted 4-hydroxy-2-quinolones
