22899-57-6 Usage
Chemical class
Oxadiazole derivative
Structure
Five-membered heterocyclic compound containing oxygen and nitrogen atoms
Substitution
4-(3,4-dimethylphenyl)group on the oxadiazol-3-amine core
Pharmacological activities
Exhibits a wide range of activities, including antimicrobial, antifungal, anti-inflammatory, and antitumor effects
Applications
Potential use in pharmaceutical and medicinal chemistry fields
Biological activities
May have promising applications due to its diverse pharmacological properties
Chemical properties
The 4-(3,4-dimethylphenyl)substitution on the core structure provides specific chemical properties
Heterocyclic compound
Contains both oxygen and nitrogen atoms in its ring structure
Derivative
A modified version of the parent compound, oxadiazole
Potential for drug development
Due to its various pharmacological activities, 1,2,5-Oxadiazol-3-amine, 4-(3,4-dimethylphenyl)- may be a candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 22899-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,9 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22899-57:
(7*2)+(6*2)+(5*8)+(4*9)+(3*9)+(2*5)+(1*7)=146
146 % 10 = 6
So 22899-57-6 is a valid CAS Registry Number.
22899-57-6Relevant academic research and scientific papers
One-pot synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans
Sheremetev
, p. 1057 - 1059 (2007/10/03)
A "one pot" method for the synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans from β-aryl- and 4-β-hetaryl-β-oxo acid esters was developed.
