10222-62-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Methoxy-quinoline-4-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and molecules with diverse therapeutic applications.
Used in Anti-inflammatory Applications:
2-Methoxy-quinoline-4-carboxylic acid is used as an anti-inflammatory agent for its potential to modulate inflammatory pathways and reduce inflammation-related symptoms. Its anti-inflammatory properties can be harnessed in the treatment of various conditions characterized by excessive inflammation.
Used in Antioxidant Applications:
As an antioxidant, 2-Methoxy-quinoline-4-carboxylic acid is used to neutralize free radicals and protect cells from oxidative damage. Its antioxidant activity can contribute to the prevention and treatment of various diseases associated with oxidative stress, such as neurodegenerative disorders and cardiovascular diseases.
Used in Antimicrobial Applications:
2-Methoxy-quinoline-4-carboxylic acid is used as a potential antibacterial and antifungal agent due to its demonstrated activity against certain bacteria and fungi. Its antimicrobial properties can be utilized in the development of new agents to combat drug-resistant infections and improve public health.
Used in Research and Development:
In the field of research and development, 2-Methoxy-quinoline-4-carboxylic acid is used as a chemical probe to study various biological processes and pathways. Its unique structure and functional groups allow researchers to investigate its interactions with biological targets and explore its potential applications in drug discovery and development.
It is crucial to handle 2-Methoxy-quinoline-4-carboxylic acid with care, as it may pose health hazards if not properly managed. Proper safety measures and precautions should be taken during its synthesis, storage, and use to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 10222-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10222-62:
(7*1)+(6*0)+(5*2)+(4*2)+(3*2)+(2*6)+(1*2)=45
45 % 10 = 5
So 10222-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c1-15-10-6-8(11(13)14)7-4-2-3-5-9(7)12-10/h2-6H,1H3,(H,13,14)
10222-62-5Relevant articles and documents
QUINOLINE DERIVATIVE HAVING SEROTONIN-3 RECEPTOR ANTAGONIZING ACTIVITY
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, (2008/06/13)
Quinoline derivatives represented by formula (I): STR1 wherein A-B-D represents--C(COO--Y)=CH--C(OR)= (wherein Y represents 8-methyl-8-azabicyclo[3.2.1]oct-3-yl group and R represents alkyl) or--C(OH)=C(COX--Y)--CH= (wherein X represents--O--or--NH--; and Y has the same meaning as described above), or a pharmaceutically acceptable salt thereof, possess potent 5HT 3 antagonizing activity and are useful as antiemetic agents.
5-HT3 Receptor Antagonists. 1. New Quinoline Derivatives
Hayashi, Hiroaki,Miwa, Yoshikazu,Miki, Ichiro,Ichikawa, Shunji,Yoda, Noboyuki,et al.
, p. 4893 - 4902 (2007/10/02)
A series of esters and amides of 1-alkyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid or 2-alkoxyquinoline-4-carboxylic acid containing a basic azabicycloalkyl moiety has been synthesized and evaluated for affinity for the 3H>quipazine-labeled
QUINOLINE SUBSTITUTED OXOMETHYL OR THIOXOMETHYL GLYCINE DERIVATIVES AND ALDOSE REDUCTASE INHIBITON THEREWITH
-
, (2008/06/13)
A compound of the formula (I): or a pharmaceutically acceptable salt thereof, wherein Y is S or O; R is hydrogen or alkyl having from about 1 to about 4carbon atoms; R1 is hydrogen, alkyl having from about 1 to about 4carbon atoms, alkoxy having from about 1 to about 4carbon atoms, halogen or trifluoromethyl; R2 is hydrogen or unsubstituted or substituted alkyl having from about 1 to about 4 carbon atoms; and R3 is hydrogen, alkyl having from about 1 to about 6carbon atoms, cycloalkyl having from about 3 to about 6 carbon atoms, alkoxy having from about 1 to about 4 carbon atoms, aryloxy having from about 6 to about 10 carbon atoms, alkylthio having from about 1 to about 4 carbon atoms, hydroxyalkoxy having from about 1 to about 4 carbon atoms, or unsubstituted or substituted phenyl is useful to obtain inhibition of aldose reduction in animals, including humans.
