64022-99-7 Usage
Type of compound
Heterocyclic organic compound
Tetrazole ring
A five-membered ring with four nitrogen atoms and one sulfur atom
Substitution
4-methylthiophenyl group attached to the tetrazole ring
Potential applications
Pharmaceutical, agrochemical, and materials science industries
Unique properties
Chemical and physical properties that make it suitable for various applications
Biological activity
The ability to interact with biological systems, potentially leading to therapeutic effects
Drug discovery
Studied as a building block for creating new pharmaceutical compounds
Synthesis
Can be used to synthesize other compounds
Coordination chemistry
Acts as a ligand, bonding with metal ions to form coordination complexes
Check Digit Verification of cas no
The CAS Registry Mumber 64022-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64022-99:
(7*6)+(6*4)+(5*0)+(4*2)+(3*2)+(2*9)+(1*9)=107
107 % 10 = 7
So 64022-99-7 is a valid CAS Registry Number.
64022-99-7Relevant academic research and scientific papers
[3+1+1] type cyclization of ClCF2COONa for the assembly of imidazoles and tetrazolesvia in situgenerated isocyanides
Song, Qiuling,Wang, Ya,Zhou, Yao
supporting information, p. 6106 - 6109 (2020/06/10)
A facile synthesis of imidazoles and tetrazolesvia[3+1+1] type cyclization of ClCF2COONa is developed. A diverse array of imidazoles and tetrazoles were obtained in decent yieldsviaisocyanide intermediates. Notably, this is the first example of the cycloaddition ofin situgenerated isocyanides.
1-(Para-substituted-phenyl)-1H-tetrazoles
-
, (2008/06/13)
This disclosure describes compounds of the class of 1-(para-substituted-phenyl)-1H-tetrazoles useful as antimicrobial agents.
