52454-63-4 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Thiazol-5-ylacetic acid is used as a pharmaceutical intermediate for the synthesis of various drug molecules. Its unique chemical structure and properties make it a valuable component in the development of new medications with potential therapeutic applications.
Used in Research and Development:
In the research industry, 1,3-Thiazol-5-ylacetic acid is utilized as a key building block in the organic synthesis of novel compounds. Its diverse range of applications and potential for creating new drug candidates contribute to the advancement of scientific knowledge and the discovery of innovative treatments.
Used in Anti-inflammatory and Antioxidant Applications:
1,3-Thiazol-5-ylacetic acid is studied for its potential as an anti-inflammatory and antioxidant agent. Its properties suggest that it may be effective in treating conditions associated with inflammation and oxidative stress, offering a promising avenue for medical intervention and treatment development.
Used in Fine Chemicals Synthesis:
1,3-Thiazol-5-ylacetic acid is also employed in the synthesis of fine chemicals, which are high-purity chemicals used in various applications, including the production of specialty products and materials. Its versatility and reactivity make it an essential component in the creation of high-quality fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 52454-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52454-63:
(7*5)+(6*2)+(5*4)+(4*5)+(3*4)+(2*6)+(1*3)=114
114 % 10 = 4
So 52454-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NO2S/c7-5(8)1-4-2-6-3-9-4/h2-3H,1H2,(H,7,8)
52454-63-4Relevant academic research and scientific papers
Methods of making 2,6-diaryl piperidine derivatives
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, (2008/06/13)
Methods for preparing 2,6-diaryl piperidine derivatives are described. More particularly, 2,6-diaryl piperidines having formula 1-4 are prepared by cyclocondensation of an aryl or heteroaryl aldehyde with 1,3-acetonedicarboxylic acid.
