14802-13-2 Usage
Uses
Used in Pharmaceutical Industry:
4(1H)-Quinolinone, 3-acetyl-2-phenylis used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its diverse range of biological activities, such as anti-inflammatory, antimicrobial, and anti-cancer properties, make it a valuable component in the development of new drugs.
Used in Neurodegenerative Disease Treatment:
4(1H)-Quinolinone, 3-acetyl-2-phenylis used as a potential therapeutic agent for the treatment of neurodegenerative diseases, such as Alzheimer's and Parkinson's. Its biological activities and potential neuroprotective effects have been studied to explore its efficacy in managing these conditions.
Used in Material Science:
4(1H)-Quinolinone, 3-acetyl-2-phenylis used as a building block in the development of new materials. Its unique chemical structure and properties make it a promising candidate for creating innovative materials with various applications.
Used in Coordination Chemistry:
4(1H)-Quinolinone, 3-acetyl-2-phenylis used as a potential ligand in coordination chemistry. Its ability to form coordination complexes with metal ions can lead to the development of new compounds with unique properties and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 14802-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,0 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14802-13:
(7*1)+(6*4)+(5*8)+(4*0)+(3*2)+(2*1)+(1*3)=82
82 % 10 = 2
So 14802-13-2 is a valid CAS Registry Number.
14802-13-2Relevant academic research and scientific papers
The Reactions of Some ortho-Substituted Anilines With Various α,β-Acetylenic Ketones. A Route to Substituted Quinolines
Sinsky, M. S.,Bass, R. G.
, p. 759 - 768 (2007/10/02)
The reactions of some ortho-substituted anilines with various α,β-acetylenic ketones were investigated as a route to 4-alkyl-, 4-aryl-, 4-hydroxy-, and 4-amino-3-quinolyl ketones.The anilines examined were 2-aminoacetophenone (1), 2-aminobenzophenone (2), anthranilonitrile (3), methyl anthranilate (4), and ethyl anthranilate (5).The acetylenic ketones used were 1,4-diphenyl-2-butyne-1,4-dione (6), 3-butyn-2-one (7), 1,3-diphenyl-2-propyn-1-one (8), and 4-phenyl-3-butyn-2-one (9).The acetylenic ketones typically reacted with the anilines to give enamines; however, exceptions were found.Acetylene 6 reacts with 3 to give the enamine (13) along with a small amount of 2,3-dibenzoyl-4-quinolamine (14).The reactions of 1 or 2 with 6 give the respective quinoline derivatives directly.Acetylene 8 reacts with 2 to give 3-benzoyl-2,4-diphenylquinoline (22) directly, whereas no reaction occurs between 8 and 1 or 3.Acetylene 9 does not react with 1, 2 or 3.The enamines exist as the intramolecularly hydrogen bonded isomers and usually undergo cyclization with 5 molar equivalents of methanolic sodium methoxide to give quinoline derivatives.The 4-quinolinols exist predominantly as the 4-quinolinone tautomer.
