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5-amino-1-(4-nitrophenyl)-1H-1,2,3-triazole-4-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103029-86-3

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103029-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103029-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,2 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103029-86:
(8*1)+(7*0)+(6*3)+(5*0)+(4*2)+(3*9)+(2*8)+(1*6)=83
83 % 10 = 3
So 103029-86-3 is a valid CAS Registry Number.

103029-86-3Relevant academic research and scientific papers

Catalytic behavior of surfactant-containing-MCM-41 mesoporousmaterials for cycloaddition of 4-nitrophenyl azide

Boukoussa, Bouhadjar,Zeghada, Sarah,Ababsa, Ghenia Bentabed,Hamacha, Rachida,Derdour, A?cha,Bengueddach, Abdelkader,Mongin, Florence

, p. 131 - 139 (2015)

Si-MCM-41, Ga-MCM-41 and Al-MCM-41 mesoporous catalysts (with Si/Al = 80 and Si/Ga = 80) were pre-pared by direct synthesis under hydrothermal crystallization method using sodium aluminate or galliumsulfate and tetraethyl orthosilicate (TEOS) as aluminum

Synthesis of biologically as well as industrially important 1,4,5-trisubstituted-1,2,3-triazoles using a highly efficient, green and recyclable DBU-H2O catalytic system

Singh, Harjinder,Sindhu, Jayant,Khurana, Jitender M.

, p. 22360 - 22366 (2013/11/06)

Substituted 1,2,3-triazoles are important heterocyclic molecules with applications in diverse research areas. 1,3-Dipolar cycloaddition reaction of azides and enolizable compounds is an important method of generating substituted 1,2,3-triazoles. However,

A combined experimental and theoretical study of the thermal cycloaddition of aryl azides with activated alkenes

Zeghada, Sarah,Bentabed-Ababsa, Ghenia,Derdour, Aicha,Abdelmounim, Safer,Domingo, Luis R.,Saez, Jose A.,Roisnel, Thierry,Nassar, Ekhlass,Mongin, Florence

experimental part, p. 4295 - 4305 (2011/07/08)

Reactions were performed from aryl azides on the one hand, and activated alkenes coming from β-dicarbonyl compounds or malonodinitrile on the other hand, either with recourse to conventional heating or to microwave activation, to afford 1-aryl-1H-1,2,3-tr

A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3- triazoles

Smith, Catherine J.,Nikbin, Nikzad,Ley, Steven V.,Lange, Heiko,Baxendale, Ian R.

supporting information; experimental part, p. 1938 - 1947 (2011/04/24)

Having demonstrated in the preceding publication the flow synthesis of aryl azides, we describe here a general protocol for the in-line purification of these versatile intermediates. As part of this investigation, we evaluated the use of ReactIR 45m as a

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