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3-benzyl-3H-[1,2,3]triazole-4-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103264-49-9

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103264-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103264-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103264-49:
(8*1)+(7*0)+(6*3)+(5*2)+(4*6)+(3*4)+(2*4)+(1*9)=89
89 % 10 = 9
So 103264-49-9 is a valid CAS Registry Number.

103264-49-9Downstream Products

103264-49-9Relevant academic research and scientific papers

On the reactivity of activated alkynes in copper and solvent-free Huisgens reaction

Elamari, Hichem,Jlalia, Ibtissem,Louet, Charlotte,Herscovici, Jean,Meganem, Faouzi,Girard, Christian

scheme or table, p. 1179 - 1183 (2010/11/02)

Terminal alkynes substituted by a carbonyl-type electron-withdrawing group have been found to undergo Huisgens cycloaddition with azides at room temperature in a solvent-free manner; without a need of either heating or catalysis. Metallic salts, other tha

Trimethylsilyl-directed 1,3-dipolar cycloaddition reactions in the solid-phase synthesis of 1,2,3-triazoles

Coats, Steven J.,Link, Jeffrey S.,Gauthier, Diane,Hlasta, Dennis J.

, p. 1469 - 1472 (2007/10/03)

(Chemical Equation Presented) A regioselective method for the preparation of 1,5-trisubstituted 1H-1,2,3-triazoles via a 1,3-dipolar cycloaddition of 1-trimethylsilylacetylenes with organoazides is described. Immobilization of the azide on REM resin and s

UNSATURATED CARBONYL-CONTAINING COMPOUNDS. XXVIII. CYCLOADDITION OF ORGANIC AZIDES TO α-ACETYLENIC KETONES AND ACIDS

Vereshchagin, L. I.,Tikhonova, L. G.,Maksikova, A. V.,Serebryakova, E. S.,Proidakov, A. G.,Filippova, T. M.

, p. 641 - 648 (2007/10/02)

The reaction of α-acetylenic ketones and acids with organic azides leads to the formation of 1-alkyl(aryl)-4-acyl(carboxy)-1,2,3-triazoles or to a mixture of the 1,4- and 1,5-disubstituted isomers.The effect of the structure of the initial compound and of the solvent on the direction of cycloaddition was investigated.

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