14179-84-1 Usage
General Description
2-Oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid is a chemical compound with the molecular formula C11H11NO3. It is a derivative of quinoline and contains both a carbonyl group and a carboxylic acid functional group. 2-Oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid has potential applications in pharmaceutical research and drug development due to its structural features, which may contribute to its biological activity and potential medicinal properties. The compound may be used as a building block in the synthesis of various organic compounds and could serve as a precursor for the development of new pharmaceutical agents targeting specific biological pathways or disease states. Further research and exploration of the chemical and its properties may reveal its potential for use in various fields including medicine, chemistry, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 14179-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14179-84:
(7*1)+(6*4)+(5*1)+(4*7)+(3*9)+(2*8)+(1*4)=111
111 % 10 = 1
So 14179-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c12-9-5-7(10(13)14)6-3-1-2-4-8(6)11-9/h1-4,7H,5H2,(H,11,12)(H,13,14)
14179-84-1Relevant articles and documents
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Zrike,Lindwall
, p. 49 (1936)
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Synthesis of substituted 1,2,3,4-tetrahydroquinoline-4-carboxylic acids
Zhuravleva,Zimichev,Zemtsova,Klimochkin
, p. 609 - 612 (2009)
Reduction of some substituted quinoline-4-carboxylic acids was studied. The reduction of 2-alkylquinoline-4-carboxylic acids with Raney nickel in aqueous alkali was stereoselective, and the resulting 2-alkyl-1,2,3,4- tetrahydroquinoline-4-carboxylic acids
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Sumpter et al.
, p. 1037 (1945)
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