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1-(3-chloro-4-fluorophenyl)-1H-1,2,3-triazole is a chemical compound with the molecular formula C7H4ClFN3. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The compound features a 3-chloro-4-fluorophenyl group attached to the triazole ring, which imparts unique electronic and steric properties. This specific arrangement of atoms and functional groups makes it a potentially valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its chemical structure and properties can be further explored for potential applications in medicinal chemistry, materials science, and other fields where novel compounds with specific reactivity or selectivity are sought.

85863-03-2

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85863-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85863-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85863-03:
(7*8)+(6*5)+(5*8)+(4*6)+(3*3)+(2*0)+(1*3)=162
162 % 10 = 2
So 85863-03-2 is a valid CAS Registry Number.

85863-03-2Downstream Products

85863-03-2Relevant academic research and scientific papers

A novel approach to 1-monosubstituted 1,2,3-triazoles by a click cycloaddition/decarboxylation process

Xu, Mei,Kuang, Chunxiang,Wang, Zhuo,Yang, Qing,Jiang, Yubo

supporting information; experimental part, p. 223 - 228 (2011/03/18)

The synthesis of 1-monosubstituted 1,2,3-triazoles was achieved using azides and propiolic acid by copper-catalyzed click cycloaddition/ decarboxylation, which was easily carried out in N,N-dimethylformamide at room temperature or 60 C with yields ranging

Facile and quick synthesis of 1-monosubstituted aryl 1,2,3-triazoles: A copper-free [3+2] cycloaddition

Jiang, Yubo,Kuang, Chunxiang,Yang, Qing

experimental part, p. 289 - 292 (2011/02/28)

An efficient copper-free synthesis of 1-monosubstituted aryl 1,2,3-triazoles from sodium acetylide and aryl azides was developed, which was found suitable for various aryl azides and completed within 15 min at room temperature with moderate to excellent y

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