415679-26-4 Usage
Uses
Used in Pharmaceutical Industry:
[5-(2-METHOXY-PHENYL)-[1,3,4]OXADIAZOL-2-YL]-ACETIC ACID is used as a building block for the development of new pharmaceuticals, leveraging its diverse biological activities and the potential for targeted drug delivery through the acetic acid group.
Used in Anticancer Applications:
In the field of oncology, [5-(2-METHOXY-PHENYL)-[1,3,4]OXADIAZOL-2-YL]-ACETIC ACID is used as a potential anticancer agent, given its association with the biological activities of oxadiazole compounds. It may be employed to target and inhibit cancer cell growth, with further research needed to explore its specific mechanisms of action and efficacy.
Used in Drug Delivery Systems:
The acetic acid group in [5-(2-METHOXY-PHENYL)-[1,3,4]OXADIAZOL-2-YL]-ACETIC ACID allows for its use as a component in drug delivery systems. It can be conjugated to other therapeutic molecules, enhancing their targeted delivery and bioavailability, which may improve the overall effectiveness of treatments in various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 415679-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,6,7 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 415679-26:
(8*4)+(7*1)+(6*5)+(5*6)+(4*7)+(3*9)+(2*2)+(1*6)=164
164 % 10 = 4
So 415679-26-4 is a valid CAS Registry Number.
415679-26-4Relevant academic research and scientific papers
Janda, Lubomir
, p. 411 - 416 (2001)
Ethyl (1H-tetrazol-5-yl)acetate is acylated with aroyl chlorides and heteroaroyl chlorides in pyridine. The intermediate acyltetrazoles undergo thermal degradation to ethyl (5-aryl-1,3,4-oxadiazol-2-yl)acetates and (5-heteroaryl-1,3,4-oxadiazol-2-yl)acetates, respectively, in good yields. The corresponding acetic acids are obtained by potassium hydroxide mediated hydrolysis of the esters in anhydrous ethanol.
