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1H-1,2,3-Triazole, 1-(3-nitrophenyl)-5-phenyl- is a complex organic compound with the molecular formula C15H10N4O2. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The compound features a 3-nitrophenyl group attached to the nitrogen atom at position 1 and a phenyl group at position 5. The nitro group (-NO2) in the 3-nitrophenyl moiety introduces an electron-withdrawing effect, which can influence the compound's reactivity and properties. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and potential to form stable complexes with metal ions. Its applications span across a range of industries, including medicine, agriculture, and materials science.

64214-89-7

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64214-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64214-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,1 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64214-89:
(7*6)+(6*4)+(5*2)+(4*1)+(3*4)+(2*8)+(1*9)=117
117 % 10 = 7
So 64214-89-7 is a valid CAS Registry Number.

64214-89-7Upstream product

64214-89-7Downstream Products

64214-89-7Relevant academic research and scientific papers

Transition-metal-free regioselective construction of 1,5-diaryl-1,2,3-triazoles through dehydrative cycloaddition of alcohols with aryl azides mediated by SO2F2

Zhang, Xu,Rakesh,Qin, Hua-Li

, p. 2845 - 2848 (2019)

A novel, simple and practical method for mild, efficient, cost-effective and regioselective synthesis of highly valuable 1,5-diaryl-1,2,3-triazoles was achieved through dehydrative annulation of readily available alcohols with aryl azides. The reaction proceeded at room temperature, without any metal catalysts, exhibiting excellent compatibility to a large variety of functional groups (>50 examples), resulting in up to quantitative yields. 2019

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