2055-53-0 Usage
Structure
1H-1,2,3-Triazole-4-carboxamide, 1-phenylis a triazole-based compound with a carboxamide functional group and a phenyl group attached to the nitrogen atom.
Functional groups
Triazole, carboxamide, and phenyl.
Potential pharmaceutical use
Exhibits antifungal, antitumor, and antiparasitic activities.
Application in synthesis
Used as a building block in the synthesis of various drugs and bioactive molecules.
Other potential applications
Studied for its potential as a corrosion inhibitor and as a ligand in coordination chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2055-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2055-53:
(6*2)+(5*0)+(4*5)+(3*5)+(2*5)+(1*3)=60
60 % 10 = 0
So 2055-53-0 is a valid CAS Registry Number.
2055-53-0Relevant academic research and scientific papers
Copper Acetate Catalyzed Regio-selective Synthesis of Substituted 1,2,3-Triazoles: A Versatile Azide–Alk-ene Cycloaddition/Oxidation Approach
Rohilla, Sandeep,Patel, Shyam Sunder,Jain, Nidhi
, p. 847 - 854 (2017/01/18)
A copper acetate catalyzed oxidative cycloaddition reaction of benzyl and aryl azides with terminal and internal olefins that contain electron-withdrawing groups (COOR, CONH2, CN, CHO, COR) has been developed. The reaction employs air as the oxidant and does not require any base or additives to afford 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles in good to excellent yields with high regioselectivity.
