53897-99-7 Usage
Chemical class
Triazole derivatives
Explanation
It belongs to a class of compounds that contain a five-membered ring structure with three nitrogen atoms.
Explanation
It contains a five-membered ring structure with three nitrogen atoms and one sulfur atom.
Explanation
It is used in various fields due to its antifungal, antimicrobial, and herbicidal properties.
Explanation
It is known for its ability to inhibit the growth of fungi.
Explanation
It can inhibit the growth of microorganisms, making it useful in the production of drugs and agricultural products.
Explanation
It is used to control the growth of unwanted plants in agricultural settings.
Explanation
It is used as a building block in the synthesis of other organic compounds.
Explanation
It has diverse applications in different industries, making it a valuable compound.
Explanation
The molecular structure of 1H-[1,2,3]TRIAZOLE-4-CARBOTHIOIC ACID AMIDE consists of a five-membered ring with three nitrogen atoms and one sulfur atom.
Heterocyclic compound
Yes
Applications
Pharmaceuticals, agrochemicals, and materials science
Anti-fungal properties
Yes
Anti-microbial properties
Yes
Herbicidal properties
Yes
Intermediate in synthesis
Yes
Versatile chemical
Yes
Structure
Five-membered ring with three nitrogen atoms and one sulfur atom
Check Digit Verification of cas no
The CAS Registry Mumber 53897-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53897-99:
(7*5)+(6*3)+(5*8)+(4*9)+(3*7)+(2*9)+(1*9)=177
177 % 10 = 7
So 53897-99-7 is a valid CAS Registry Number.
53897-99-7Relevant academic research and scientific papers
Rhodium acetate catalyzed and thermal reactions of 6-alkoxy-5-diazodihydrouracils
Mathur, Naresh C.,Shechter, Harold
, p. 3799 - 3802 (2007/10/02)
6-Alkoxy-5-diazodihydrouracils are converted by rhodium acetate to 5-(alkoxyrnethylene)- 2,4-imidazolidinediones and thermolyze to 1,2,3-triazole-4-carboxamide derivatives.
TRANSFORMATIONS OF SUBSTITUTED 5-AMINOPYRIMIDINES UNDER CONDITIONS OF THE DIAZOTIZATION
Nemeryuk, Michal P.,Sedov, Andrej L.,Safonova, Tamara S.,Cerny, Antonin,Krepelka, Jiri
, p. 215 - 233 (2007/10/02)
Reaction of nitrous acid with 4-substituted and 4,6-disubstituted 5-aminopyrimidines Ia-In produces 4-substituted and 4,5-disubstituted 1,2,3-triazoles IIa-IIv, resp.Under similar conditions, 2,5-diaminopyrimidines XIIa-XIId give N(7)-oxides of 2-amino-4-aralkylthiopyrimido-1,2,3-triazines XIIIa-XIIId, and 5-amino-4-chloropyrimidines In and X give 2-diazocyanoacetamides XIa and XIb, resp.Also described are syntheses of 5-formylaminopyrimidines XVa-XVg from glycine ethyl ester via sodium salt XVI.
