592534-87-7 Usage
Molecular structure
The compound has a complex molecular structure, containing a tetrazinone ring, a dimethylpyrazole group, and a bromophenylethylidenehydrazone moiety.
Potential applications
The compound has potential applications in various fields, including pharmaceuticals, materials science, and chemical research.
Synthesis
The synthesis of the compound is important for further understanding and potential utilization in various chemical and biological processes.
Characterization
The characterization of the compound is important for understanding its properties and potential applications.
Chemical properties
The compound may have unique chemical properties due to its complex molecular structure.
Biological properties
The compound may have unique biological properties due to its complex molecular structure.
Stability
The stability of the compound may be influenced by factors such as temperature, pH, and exposure to light.
Solubility
The solubility of the compound may be influenced by factors such as the solvent used and the compound's molecular structure.
Reactivity
The reactivity of the compound may be influenced by factors such as the presence of other chemicals and the compound's molecular structure.
Safety
The safety of the compound should be considered when handling and using it, as it may have potential hazards or risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 592534-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,2,5,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 592534-87:
(8*5)+(7*9)+(6*2)+(5*5)+(4*3)+(3*4)+(2*8)+(1*7)=187
187 % 10 = 7
So 592534-87-7 is a valid CAS Registry Number.
592534-87-7Relevant academic research and scientific papers
Cyclization of (1,2,4,5-tetrazin-3-yl)hydrazones to 3,7-dihydro-1,2,4- triazolo[4,3-b]-1,2,4,5-tetrazines
Tolshchina,Vyakhireva,Ignatenko,Ishmetova,Ganebnykh,Slepukhin,Rusinov
scheme or table, p. 1281 - 1290 (2010/10/04)
The intramolecular cyclization of (6-R-1,2,4,5-tetrazin-3-yl)hydrazones of ketones (R is 3,5-dimethylpyrazol-1-yl, 4-methylimidazol-1-yl, or 2-alkylidenehydrazino) giving rise to the previously unknown ,7-dihydro-1,2,4-triazolo[4,3-b]-1,2,4,5-tetrazines, including spiro com-pounds, was studied. The reactivity and the yields of the reaction products depend on the structure of the alkylidene fragment and the nature of the substituent in the tetrazine ring. ; 2009 Springer Science+Business Media, Inc.
