233-59-0 Usage
Description
2H-naphtho[1,2-d][1,2,3]triazole, also known as Naphthalen-2-yl-[1,2,3]triazole, is a heterocyclic compound characterized by a naphthalene ring fused to a triazole ring. It is widely recognized in the field of organic chemistry for its role as a building block in the synthesis of new organic compounds with potential biological activities. This chemical is noted for its high stability and has been a subject of interest in materials science for its potential use in organic semiconductors and optoelectronic devices. Furthermore, research has indicated that derivatives of 2H-naphtho[1,2-d][1,2,3]triazole may possess anti-cancer and anti-microbial properties.
Uses
Used in Organic Chemistry:
2H-naphtho[1,2-d][1,2,3]triazole is used as a building block for synthesizing new organic compounds with potential biological activities, due to its unique structure and stability.
Used in Materials Science:
In the field of materials science, 2H-naphtho[1,2-d][1,2,3]triazole is utilized in the development of organic semiconductors and optoelectronic devices, capitalizing on its stability and electronic properties.
Used in Pharmaceutical Research:
2H-naphtho[1,2-d][1,2,3]triazole derivatives are studied for their potential as anti-cancer and anti-microbial agents, showing promise in various research studies for their therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 233-59-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 233-59:
(5*2)+(4*3)+(3*3)+(2*5)+(1*9)=50
50 % 10 = 0
So 233-59-0 is a valid CAS Registry Number.
233-59-0Relevant articles and documents
Selective Synthesis of N-H and N-Aryl Benzotriazoles by the [3 + 2] Annulation of Sodium Azide with Arynes
Guin, Avishek,Gaykar, Rahul N.,Bhattacharjee, Subrata,Biju, Akkattu T.
, p. 12692 - 12699 (2019/10/11)
The synthetic utility of NaN3 as the azide component in the [3 + 2] annulation with arynes generated from 2-(trimethylsilyl)aryltriflates resulting in the transition-metal-free synthesis of N-H and N-aryl benzotriazoles has been demonstrated. Using CsF as the fluoride source in CH3CN, the N-H benzotriazoles are formed in high selectivity instead of the expected azidobenzene. Interestingly, N-aryl benzotriazoles are formed using KF and THF as solvent in an open-flask reaction. Moreover, a method for the N1-arylation of benzotriazole is also presented.
Compounds and methods
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, (2008/06/13)
Compounds of this invention are non-peptide, reversible inhibitors of type 2 methionine aminopeptidase, useful in treating conditions mediated by angiogenesis, such as cancer, haemangioma, proliferative retinophathy, rheumatoid arthritis, atherosclerotic
