6219-58-5 Usage
Uses
Used in Organic Synthesis:
3-(2-Aminophenyl)-[1,2,4]triazole is used as a building block for the synthesis of various organic compounds. Its stable structure and the presence of nitrogen atoms make it a valuable component in the creation of complex molecules, which can be utilized in different industries.
Used in Pharmaceutical Industry:
3-(2-Aminophenyl)-[1,2,4]triazole is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, contributing to the advancement of medicine.
Used in Chemical Research:
3-(2-Aminophenyl)-[1,2,4]triazole is used as a research tool in the field of chemistry. Its properties and reactivity can be studied to gain insights into the behavior of similar compounds, leading to the discovery of new chemical reactions and processes.
Used in Material Science:
3-(2-Aminophenyl)-[1,2,4]triazole is used as a component in the development of new materials with specific properties. Its stable structure and the ability to form various chemical bonds make it a candidate for creating materials with applications in electronics, coatings, and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6219-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6219-58:
(6*6)+(5*2)+(4*1)+(3*9)+(2*5)+(1*8)=95
95 % 10 = 5
So 6219-58-5 is a valid CAS Registry Number.
6219-58-5Relevant academic research and scientific papers
Imidazoline derivatives as alpha-1A adrenoceptor ligands
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Page/Page column 35, (2010/02/11)
Compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof are disclosed. Such compounds are useful in the treatment of Alpha-1A mediated diseases or conditions such as urinary incontinence.
2-(Anilinomethyl)imidazolines as α1 adrenergic receptor agonists: α1a subtype selective 2′-heteroaryl compounds
Speake, Jason D.,Navas III, Frank,Bishop, Michael J.,Garrison, Deanna T.,Bigham, Eric C.,Hodson, Stephen J.,Saussy, David L.,Liacos, Jim A.,Irving, Paul E.,Sherman, Bryan W.
, p. 1183 - 1186 (2007/10/03)
The structure-activity relationship of 2′-pyrrole, pyrazole and triazole substituted 2-(anilinomethyl)imidazolines as α1 adrenergic agonists was investigated. The size and orientation of substituents, as well as the position of the heteroatoms, were found to have a profound effect on the potency and selectivity of the molecules. Potent α1A subtype selective agonists have been identified.
5-(2-Aminophenyl)-s-triazoles
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, (2008/06/13)
Anti-inflammatory agents of the formula: STR1 wherein R° is hydrogen, halo, alkoxy, alkyl, or CF3 or two adjacent R° together may also form methylenedioxy, R is hydrogen or lower alkyl, and n is 1 or 2.
