83553-13-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Acetonyl-5-methyl-1,3,4-oxadiazole is used as an antimicrobial agent for its potential to combat bacterial and fungal infections. Its research-backed properties make it a promising candidate for the development of new antibiotics and antifungal medications, addressing the growing need for effective treatments against drug-resistant pathogens.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory drug development, 2-Acetonyl-5-methyl-1,3,4-oxadiazole is utilized as a non-steroidal anti-inflammatory drug candidate. Its demonstrated anti-inflammatory effects position it as a potential alternative to traditional NSAIDs, offering a new avenue for the treatment of inflammation-related conditions without the side effects associated with steroidal treatments.
Used in Drug Development Research:
2-Acetonyl-5-methyl-1,3,4-oxadiazole is employed as a subject of interest in drug development research. Its unique chemical structure and properties are being studied to explore its potential in the creation of novel therapeutic agents, particularly in the areas of infectious disease treatment and inflammation management.
Check Digit Verification of cas no
The CAS Registry Mumber 83553-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,5 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83553-13:
(7*8)+(6*3)+(5*5)+(4*5)+(3*3)+(2*1)+(1*3)=133
133 % 10 = 3
So 83553-13-3 is a valid CAS Registry Number.
83553-13-3Relevant academic research and scientific papers
New Acetonylsubstituted Azoles, II. 2-Acetonyl-1,2,4-oxadiazoles, 2-Acetonyl-1,3,4-oxadiazoles and 5-Acetonyl-1,2,4-thiadiazoles
Kuebel, Boerries
, p. 793 - 804 (2007/10/02)
3-Acetonyl-1,2,4-oxadiazoles and 2-Acetonyl-1,3,4-oxadiazoles are accessible starting with the ketal of acetoacetamide oxime and the ketal of acetoacetic acid hydrazide, respectively. 5-Acetonyl-1,2,4-thiadiazoles are obtained from 5-chloro-1,2,4-thiadiaz