4080-83-5 Usage
Uses
Used in Pharmaceutical Industry:
3-(3-acetamidophenyl)propanoic acid is used as an active pharmaceutical ingredient for the development of medications aimed at pain relief. It is particularly effective in conditions such as arthritis, menstrual cramps, and other inflammatory disorders due to its ability to reduce inflammation and alleviate pain.
Used in Pain Management:
As an analgesic, 3-(3-acetamidophenyl)propanoic acid is utilized for managing mild to moderate pain by reducing the prostaglandin levels that cause discomfort.
Used in Anti-inflammatory Treatments:
3-(3-acetamidophenyl)propanoic acid serves as an anti-inflammatory agent, reducing inflammation in the body and providing relief in inflammatory conditions.
Used in Antipyretic Formulations:
3-(3-acetaMidophenyl)propanoic acid is also used in antipyretic formulations to reduce fever by lowering the body's temperature set point, thus providing relief from the symptoms of fever associated with various illnesses.
Check Digit Verification of cas no
The CAS Registry Mumber 4080-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4080-83:
(6*4)+(5*0)+(4*8)+(3*0)+(2*8)+(1*3)=75
75 % 10 = 5
So 4080-83-5 is a valid CAS Registry Number.
4080-83-5Relevant academic research and scientific papers
Aryne as protein kinase inhibitors of such derivative and its medical uses
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Paragraph 0198-0200, (2016/10/08)
Disclosed is an aromatic alkyne derivative as a protein kinase inhibitor. The compound is a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof, wherein R1, R2, R3, R4, ring A, ring B, L, m, n, p or q are as specifically defin
Monoquaternary neuromuscular blocking agents based on 1 tetralone and 1 indanone
Biggs,Casy,Chu,Coutts
, p. 472 - 475 (2007/10/06)
The preparation of three isomeric 1 tetralone hydrazones and three isomeric 1 indanone hydrazones possessing a single quaternary ammonium center is described. Several of the compounds possessed significant neuromuscular blocking activity, and two approached suxamethonium in potency. 1H NMR evidence obtained from a study of the N,N dimethylhydrazones indicated that the hydrazones adopted an E configuration in solution.
