19829-79-9 Usage
Description
8-HYDROXYQUINOLINE-7-CARBOXYLIC ACID is an organic compound with the molecular formula C10H7NO4. It is characterized by its quinoline ring structure with a hydroxyl group at the 8th position and a carboxylic acid group at the 7th position. 8-HYDROXYQUINOLINE-7-CARBOXYLIC ACID has potential applications in various fields due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
8-HYDROXYQUINOLINE-7-CARBOXYLIC ACID is used as a small molecule therapeutic agent compound for its potential medicinal properties. It may be utilized in the development of new drugs targeting specific diseases or conditions, thanks to its ability to interact with biological targets and modulate various biological pathways.
Used in Chemical Research:
8-HYDROXYQUINOLINE-7-CARBOXYLIC ACID can also be used as a starting material or intermediate in the synthesis of more complex organic compounds for various applications, including the development of new pharmaceuticals, agrochemicals, or other specialty chemicals.
Please note that the provided materials do not specify the exact application reasons for 8-HYDROXYQUINOLINE-7-CARBOXYLIC ACID, so the uses listed above are general possibilities based on its classification as a small molecule therapeutic agent compound. Further research and development would be required to determine its specific applications and efficacy in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19829-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19829-79:
(7*1)+(6*9)+(5*8)+(4*2)+(3*9)+(2*7)+(1*9)=159
159 % 10 = 9
So 19829-79-9 is a valid CAS Registry Number.
19829-79-9Relevant articles and documents
O-TRENSOX: A promising water-soluble iron chelator (both Fe(III) and Fe(II)) potentially suitable for plant nutrition and iron chelation therapy
Baret,Beguin,Boukhalfa,Caris,Laulhere,Pierre,Serratrice
, p. 9760 - 9761 (1995)
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Aroylaniline compounds, pharmaceutical compositions, and methods of using same to inhibit viral activity
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, (2008/06/13)
Aroylaniline compounds which exhibit anti-retroviral activity, pharmaceutical compositions containing such aroylaniline compounds, and methods for treating a retroviral-infected host comprising administering an antiviral effective amount of an aroylaniline compound to a host.
SYNTHESIS OF QUINOLIN-8-OL-7-CARBOXYLIC ACID BY CARBOXYLATION OF QUINOLIN-8-OL
Ragulin, V. V.,Ragulina, I. R.,Shakirov, L. G.
, p. 1086 - 1088 (2007/10/03)
A study has been made of carboxylation of quinolin-8-ol and its alkali metal salts.The optimal carboxylation conditions have been determined, which ensure a yield of quinolin-8-ol-7-carboxylic acid as high as 59.5percent based on the starting material.