5533-43-7 Usage
Uses
Used in Pharmaceutical Industry:
5-hydrazino-1-phenyl-1H-tetrazole is utilized as a pharmaceutical ingredient due to its demonstrated biological activity. Its unique structure and properties make it a candidate for the development of new drugs, particularly in the context of medicinal chemistry where its potential therapeutic applications are being investigated.
Used in Propellant Industry:
In the propellant industry, 5-hydrazino-1-phenyl-1H-tetrazole is considered for its use as a high-energy material. Its capacity to release energy makes it a candidate for applications in propulsion systems, where high-energy materials are crucial for performance enhancement.
Used in Explosives Industry:
Similarly, within the explosives industry, 5-hydrazino-1-phenyl-1H-tetrazole is studied for its potential as a component in high-energy explosives. 5-hydrazino-1-phenyl-1H-tetrazole's ability to deliver a significant amount of energy upon detonation positions it as a possible ingredient in the development of more powerful explosive formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 5533-43-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,3 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5533-43:
(6*5)+(5*5)+(4*3)+(3*3)+(2*4)+(1*3)=87
87 % 10 = 7
So 5533-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N6/c8-9-7-10-11-12-13(7)6-4-2-1-3-5-6/h1-5H,8H2,(H,9,10,12)
5533-43-7Relevant academic research and scientific papers
Synthesis of some derivatives of pyrimido[5,4-e]tetrazolo[5,1-c][1,2,4]triazine; a novel heterocyclic system
Noorolahian, Negin,Shiri, Ali
, p. 609 - 611 (2015/11/27)
Several new derivatives of pyrimido[5,4-e]tetrazolo[5,1-c][1,2,4]triazine have been synthesised through the reaction of 5-hydrazinyl-1H-tetrazole with 5-bromo-2,4-dichloro-6-methylpyrimidine in CHCl3 solution at ambient conditions. Further trea
Design, synthesis and biological activity of novel non-peptidyl endothelin converting enzyme inhibitors, 1-phenyl-tetrazole-formazan analogues
Yamazaki, Kazuto,Hasegawa, Hirohiko,Umekawa, Kayo,Ueki, Yasuyuki,Ohashi, Naohito,Kanaoka, Masaharu
, p. 1275 - 1278 (2007/10/03)
A novel non-peptidyl endothelin converting enzyme inhibitor was obtained through a pharmacophore analysis of known inhibitors and three-dimensional structure database search. Analogues of the new inhibitor were designed using the structure-activity relationship of known inhibitors and synthesized. In anesthetized rats, intraperitoneal administration of the analogues suppressed the pressor responses induced by big endothelin-1.
