21744-55-8 Usage
Uses
Used in Propellant Industry:
5-Methylsulfonyltetrazole is used as a propellant in gas generator systems for its high-energy and thermally stable characteristics, contributing to the efficient functioning of these systems.
Used in Pyrotechnic Industry:
In the pyrotechnic industry, 5-Methylsulfonyltetrazole serves as a replacement for lead styphnate in percussion primers, offering an environmentally friendly and efficient alternative.
Used in Pharmaceutical Industry:
5-Methylsulfonyltetrazole is used as a pharmaceutical compound for its anti-inflammatory and analgesic properties, making it a candidate for the development of new medications to treat pain and inflammation.
Used in Energetic Materials Research:
As a potential precursor for producing nitrogen-rich energetic materials, 5-Methylsulfonyltetrazole is utilized in research and development for creating advanced materials with high energy content and stability.
Check Digit Verification of cas no
The CAS Registry Mumber 21744-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,4 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21744-55:
(7*2)+(6*1)+(5*7)+(4*4)+(3*4)+(2*5)+(1*5)=98
98 % 10 = 8
So 21744-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H4N4O2S/c1-9(7,8)2-3-5-6-4-2/h1H3,(H,3,4,5,6)
21744-55-8Relevant academic research and scientific papers
HETEROARYLS AMIDE DERIVATIVES AND THEIR USE AS GLUCOKINASE ACTIVATORS
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Page/Page column 44-45, (2010/04/06)
The present invention provides Formula (1A) compounds that act as glucokinase activators; pharmaceutical compositions thereof; and methods of treating diseases, disorders, or conditions mediated by glucokinase. X, Y, Z, R1, R2, R3, and R4 are as described herein.
Tetrazoles. XXXIV. Chemical Properties of 5-Alkyl(aryl)thiotetrazoles
Alam,Koldobskii
, p. 1149 - 1155 (2007/10/03)
Alkylation of 5-alkyl(aryl)thiotetrazoles with dimethyl sulfate under the phase transfer catalysis conditions affords isomeric 1-methyl- and 2-methyltetrazoles. The nature of the substituents at the sulfur atom does not much affect the selectivity of the reaction. When treated with anhydride of benzoic acid 5-alkyl-(aryl)thiotetrazoles are transformed into 2-alkyl(aryl)thio-5-phenyl-1,3,4-oxadiazoles, and on oxidation with potassium permanganate in the two-phase system chloroform-aqueous acetic acid in the presence of tetrabutylammonium bromide they are converted into the corresponding 5-alkyl(aryl)sulfonylderivatives.
