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2-(4-fluorophenyl)-2H-naphtho[1,2-d][1,2,3]triazole is a complex organic chemical compound with the molecular formula C17H10FN3. It is a derivative of naphtho[1,2-d][1,2,3]triazole, which is a fused-ring heterocyclic compound. The structure of 2-(4-fluorophenyl)-2H-naphtho[1,2-d][1,2,3]triazole features a naphthalene core with a triazole ring attached at the 1,2-d position, and a 4-fluorophenyl group at the 2-position. 2-(4-fluorophenyl)-2H-naphtho[1,2-d][1,2,3]triazole is of interest in the field of medicinal chemistry and materials science due to its potential applications in the development of new drugs and as a building block for various chemical syntheses. Its unique structure and properties make it a valuable compound for further research and exploration in the realm of organic chemistry.

2838-15-5

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2838-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2838-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,3 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2838-15:
(6*2)+(5*8)+(4*3)+(3*8)+(2*1)+(1*5)=95
95 % 10 = 5
So 2838-15-5 is a valid CAS Registry Number.

2838-15-5Downstream Products

2838-15-5Relevant academic research and scientific papers

Copper-Catalyzed Cyclization of Aryl Amines and Aryldiazonium Salts under Air: Access to N-2-Aryl-Naphthotriazoles

Zhu, Chuanle,Zeng, Hao,Chen, Fulin,Liu, Chi,Jiang, Huanfeng

, p. 5149 - 5159 (2019)

A catalytic and step economic protocol for the construction of N-2-aryl-naphthotriazoles via copper-catalyzed cyclization of aryl amines and aryldiazonium salts is reported. With dioxygen in the air as termial oxidants under copper catalysis, various N-2-aryl-naphthotriazoles were synthesized in high yields. Importantly, this protocol features the sufficient inhibition of the classic C-N2 bond cleavage process of aryldiazonium tetrafluoroborates under copper catalysis and the undesired dehydrogenative coupling of aryl amines under oxidative conditions. Preliminary mechanistic studies indicated that a radical procedure might not be involved in this transformation. In addition, simple decoration of the obtained compounds delivers novel and attractive tetraphenylethylene moiety containing N-2-aryl-naphthotriazole derivatives. (Figure presented.).

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