89333-94-8 Usage
Chemical Family
Oxadiazole derivatives
Molecular Weight
390.29 g/mol
Biological and Pharmacological Activities
Antimicrobial
Antiviral
Antitumor
Anti-inflammatory
Applications
Organic synthesis
Drug discovery
Chemical Reactivity
Diverse
Therapeutic Applications
Potential for further research and development in the pharmaceutical industry
Activity against Biological Targets
Exhibits activity against various targets, making it a promising candidate for research and development
Check Digit Verification of cas no
The CAS Registry Mumber 89333-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89333-94:
(7*8)+(6*9)+(5*3)+(4*3)+(3*3)+(2*9)+(1*4)=168
168 % 10 = 8
So 89333-94-8 is a valid CAS Registry Number.
89333-94-8Relevant articles and documents
1,3-Dipolar Cycloaddition Reactions of Nitrilium Betaines with Aryl Thiocyanates and Selenocyanates
Greig, Derek J.,Hamilton, Douglas G.,McPherson, Michael,Paton, R. Michael,Crosby, John
, p. 607 - 612 (2007/10/02)
The carbon-nitrogen triple bond of aryl thiocyanates acts as a dipolarophile in 1,3-dipolar cycloadditions.Reaction with nitrile oxides, nitrile sulphides, and benzonitrile N-phenylimide yields, respectively, 5-arylthio-1,2,4-oxadiazoles, -thidiazoles and -triazoles.Aryl selenocyanates behave similarly forming 5-arylseleno-1,2,4-oxadiazoles and -thiadiazoles from nitrile oxides and sulphides.Divergent pathways are followed by the reactions of secondary amines such as piperidine with 5-arylthio-1,2,4-oxadiazoles and -thidiazoles, the former yielding 5-piperidyl-1,2,4-oxadiazoles and the latter dihydro-1,2,4-thiadiazole-5-thiones.
