54503-17-2 Usage
Uses
Used in Pharmaceutical Industry:
3-AMINO-3-(4-METHOXY-3-METHYLPHENYL)PROPANOIC ACID is used as an analgesic and anti-inflammatory agent for the treatment of mild to moderate pain, including menstrual pain, arthritis, and dental pain. Its application is based on its ability to reduce inflammation and alleviate pain by inhibiting prostaglandin production.
Used in Oncology Research:
In the field of oncology, 3-AMINO-3-(4-METHOXY-3-METHYLPHENYL)PROPANOIC ACID is used as a subject of investigation for its potential anti-cancer properties. Studies are being conducted to explore its effectiveness against various types of cancer, with preliminary results indicating promise.
However, it is important to note that Meclofenamic Acid, like other NSAIDs, can have side effects such as gastrointestinal irritation, kidney problems, and an increased risk of heart attacks and strokes. Therefore, its use should be approached with caution and under the guidance of a medical professional.
Check Digit Verification of cas no
The CAS Registry Mumber 54503-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,0 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54503-17:
(7*5)+(6*4)+(5*5)+(4*0)+(3*3)+(2*1)+(1*7)=102
102 % 10 = 2
So 54503-17-2 is a valid CAS Registry Number.
54503-17-2Relevant academic research and scientific papers
A one-pot synthesis of 3-amino-3-arylpropionic acids
Tan,Weaver
, p. 7449 - 7461 (2007/10/03)
3-Aminopropionic acids (β-amino acids) are biologically active compounds of interest in medicinal and pharmaceutical chemistry. Twenty-one 3-amino-3-arylpropionic acids were synthesized via a facile one-pot synthesis. In addition, a series of mechanistic studies have been performed to optimize the production of these β-amino acids. The reaction mechanism of this one-pot synthesis of β-amino acids, as well as the electronic effect of para-substitution and the influence of solvent polarity on the proposed reaction mechanism are discussed.
