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1-(4-chlorophenyl)-5-methyl-N-phenyl-1H-1,2,3-triazole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94206-97-0

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94206-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94206-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,0 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94206-97:
(7*9)+(6*4)+(5*2)+(4*0)+(3*6)+(2*9)+(1*7)=140
140 % 10 = 0
So 94206-97-0 is a valid CAS Registry Number.

94206-97-0Downstream Products

94206-97-0Relevant academic research and scientific papers

Sonochemistry in organocatalytic enamine-azide [3+2] cycloadditions: A rapid alternative for the synthesis of 1,2,3-triazoyl carboxamides

Xavier, Daiane M.,Goldani, Bruna S.,Seus, Natália,Jacob, Raquel G.,Barcellos, Thiago,Paix?o, Márcio W.,Luque, Rafael,Alves, Diego

, p. 107 - 114 (2016/06/01)

We described herein the use of sonochemistry in the organocatalytic enamine-azide [3+2] cycloadditions of β-oxo-amides with a range of substituted aryl azides. These sonochemical promoted reactions were found to be amenable to a range of β-oxo amides or a

Organocatalytic 1,3-Dipolar Cycloaddition Reaction of β-Keto Amides with Azides - Direct Access to 1,4,5-Trisubstituted 1,2,3-Triazole-4-carboxamides

Zhou, Xiao,Xu, Xianhong,Liu, Kun,Gao, Hua,Wang, Wei,Li, Wenjun

supporting information, p. 1886 - 1890 (2016/05/09)

Organocatalytic [3+2] 1,3-dipolar cycloaddition reactions of β-keto amides with azides catalyzed by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) have been developed. This strategy generates 1,4,5-trisubstituted 1,2,3-triazole-4-carboxamides in high yields and

Synthetic method of 1,4,5-trisubstituted-1,2,3-triazole compound

-

Paragraph 0014, (2016/10/07)

The invention discloses a synthetic method of a 1,4,5-trisubstituted-1,2,3-triazole compound. In a reaction solvent, acetoacetamide and nitrine are used as reaction materials and Lewis base is used as a catalyst to carry out a reaction so as to obtain a p

Intramolecular hydrogen bonding-assisted cyclocondensation of α-diazoketones with various amines: A strategy for highly efficient Wolff 1,2,3-triazole synthesis

Wang, Zikun,Bi, Xihe,Liao, Peiqiu,Zhang, Rui,Liang, Yongjiu,Dong, Dewen

supporting information; experimental part, p. 7076 - 7078 (2012/08/14)

A catalytic and highly efficient Wolff's cyclocondensation of α-diazoketones with aromatic and aliphatic amines has been realized for the first time by utilizing the strategy of an intramolecular hydrogen bonding-activating carbonyl group. This approach successfully solved the challenging problem of poor condensation efficiency in Wolff 1,2,3-triazole synthesis, and constitutes a powerful method for the synthesis of highly functionalized 1,2,3-triazoles. The Royal Society of Chemistry 2012.

The study on synthesis of some new 1,2,3-triazolylurea and carbonyl amide derivatives

Dong, Heng-Shan,Liu, Shi-Qiang

, p. 1215 - 1219 (2007/10/03)

The study on syntheses of some N-substituted-N′-[5-methyl-1-(4- chlorophenyl)-1,2,3-triazol-4-yl]-urea 6a-e and N-substituted-[5-methyl-1-(4- chlorophenyl)-1,2,3-triazol-4-yl]carbonyl amide 6f-1 derivatives were reported in this paper. The yielded products 6a-1 were confirmed by elemental analyses, NMR, MS and IR spectra.

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