73396-58-4 Usage
Uses
Used in Corrosion Inhibition:
4-Amino-5-tert-butyl-4H-1,2,4-triazole-3-thiol is used as a corrosion inhibitor for copper, protecting it from degradation and extending its lifespan in various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4-Amino-5-tert-butyl-4H-1,2,4-triazole-3-thiol serves as an intermediate in the synthesis of various organic compounds and pharmaceuticals, contributing to the development of new drugs and treatments.
Used in Antimicrobial Applications:
Leveraging its antimicrobial properties, 4-Amino-5-tert-butyl-4H-1,2,4-triazole-3-thiol is used as an antimicrobial agent in different industries to prevent the growth of harmful microorganisms and ensure product safety and quality.
Used in Antifungal Applications:
4-Amino-5-tert-butyl-4H-1,2,4-triazole-3-thiol is employed as an antifungal agent, helping to control fungal growth and protect materials and products from fungal contamination.
Used in Antioxidant Applications:
Due to its antioxidant properties, 4-Amino-5-tert-butyl-4H-1,2,4-triazole-3-thiol is used to prevent oxidation in various chemical processes and products, thereby enhancing their stability and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 73396-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,9 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73396-58:
(7*7)+(6*3)+(5*3)+(4*9)+(3*6)+(2*5)+(1*8)=154
154 % 10 = 4
So 73396-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N4S/c1-6(2,3)4-8-9-5(11)10(4)7/h7H2,1-3H3,(H,9,11)
73396-58-4Relevant academic research and scientific papers
7H-Triazolothiazin-7-ones by Deamination Cyclization of S-Acrylates of 4-Amino-3(3H)-1,2,4-triazolethiones
Heindel, Ned D.,Reid, Jack R.
, p. 2479 - 2482 (2007/10/02)
Condensation of 4-amino-3(3H)-1,2,4-triazolethiones with methyl propiolate gave S-acrylic esters.S-Acrylic acids prepared from these esters underwent a deamination cyclization of 7H-triazolothiazin-7-ones with the loss of the elements o
