3176-52-1 Usage
Uses
Used in Pharmaceutical Industry:
3-Ethyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine is used as a pharmaceutical compound for its potential biological and pharmacological activities. Its unique structure and functional groups contribute to its possible use in the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 3-Ethyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine is used as a building block or intermediate for the synthesis of more complex organic molecules. Its presence of an ethyl and amine group allows for various chemical reactions to create a wide range of compounds.
Used in Material Science:
3-Ethyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine is also used in material science for the development of new materials with specific properties. Its incorporation into materials may lead to advancements in areas such as polymers, coatings, or sensors, depending on the desired characteristics and applications.
While further research is necessary to fully understand the properties and potential uses of 3-ethyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine, it shows promise as a valuable chemical compound with diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3176-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3176-52:
(6*3)+(5*1)+(4*7)+(3*6)+(2*5)+(1*2)=81
81 % 10 = 1
So 3176-52-1 is a valid CAS Registry Number.
3176-52-1Relevant academic research and scientific papers
Novel bridgehead nitrogen heterocyclic systems: Synthesis and antimicrobial activity of imidazo[1,2-d]-s-triazolo[3,4-b][1,3,4]thiadiazoles
Mohan, Jag,Kataria, Sangeeta
, p. 713 - 714 (2007/10/03)
A facile synthesis of 7-aryl-3-ethylimidazo[1,2-d]-s-triazolo[3,4-b][1,3,4]thiadiazole 3 has been achieved by the condensation of 4-amino-3-ethyl-5-mercapto-s-triazole 1 with cyanogen bromide to yield 6-amino-3-ethyl-s-triazolo[3,4-b][1,3,4]thiadiazole 2 followed by treatment with α-haloketones. The structures 3 are supported by IR and 1H NMR spectral data. The antibacterial and antifungal activities of the system have also been evaluated.
