31282-90-3 Usage
Uses
Used in Pharmaceutical Industry:
3-(2-Bromo-4-ethoxy-5-methoxyphenyl)propanoic acid is used as a pharmaceutical compound for its potential anti-inflammatory and analgesic effects, due to its structural similarities with ibuprofen. It is intended for the treatment of pain, fever, and inflammation, offering an alternative for patients who may require different formulations or derivatives of traditional nonsteroidal anti-inflammatory drugs (NSAIDs).
Used in Research and Development:
In the field of medicinal chemistry, 3-(2-Bromo-4-ethoxy-5-methoxyphenyl)propanoic acid serves as a subject for research and development, allowing scientists to explore its pharmacological properties, mechanism of action, and potential therapeutic applications. This may lead to the discovery of new treatments for various inflammatory conditions and pain management strategies.
Used in Drug Formulation:
3-(2-Bromo-4-ethoxy-5-methoxyphenyl)propanoic acid may be utilized in the development of drug formulations, such as tablets, capsules, or topical applications, to provide patients with convenient and effective options for managing pain and inflammation. Its unique chemical structure could potentially offer advantages in terms of bioavailability, stability, or targeted delivery compared to existing NSAIDs.
Check Digit Verification of cas no
The CAS Registry Mumber 31282-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31282-90:
(7*3)+(6*1)+(5*2)+(4*8)+(3*2)+(2*9)+(1*0)=93
93 % 10 = 3
So 31282-90-3 is a valid CAS Registry Number.
31282-90-3Relevant academic research and scientific papers
Synthesis of N-Substituted Condensed Tetrahydropyridine-Based Enaminones via Palladium-Catalyzed Intramolecular C–N Cross-coupling
Dou?ová, Hana,R??i?ková, Zdeňka,?im?nek, Petr
, p. 670 - 684 (2018/01/22)
A number of β-enaminones with secondary amino group (alkyl, cyclopropyl, and aryl) were prepared from corresponding β-diketones. Two general protocols for their palladium-catalyzed intramolecular C–N cross-coupling were established to give corresponding N-substituted condensed tetrahydropyridines in good yields. The methodology is applicable for a wide variety of structural motifs. The work also extends the applicability of novel, recently established, palladium precatalysts to new substrates.
