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

126800-12-2

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126800-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126800-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,0 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126800-12:
(8*1)+(7*2)+(6*6)+(5*8)+(4*0)+(3*0)+(2*1)+(1*2)=102
102 % 10 = 2
So 126800-12-2 is a valid CAS Registry Number.

126800-12-2Downstream Products

126800-12-2Relevant academic research and scientific papers

Multi-component reaction for the preparation of 1,5-disubstituted 1,2,3-triazoles by in-situ generation of azides and nickel-catalyzed azide-alkyne cycloaddition

Camberlein, Virgyl,Kraupner, Nicolas,Bou Karroum, Nour,Lipka, Emmanuelle,Deprez-Poulain, Rebecca,Deprez, Benoit,Bosc, Damien

supporting information, (2021/05/10)

An efficient one-pot procedure combining bromide conversion into azide followed by NiAAC for the preparation of 1,5-disubstituted 1,2,3-triazoles has been developed. This procedure prevents the use of isolated azides, which are insufficiently commercially

A tunable route to oxidative and eliminative [3+2] cycloadditions of organic azides with nitroolefins: CuO nanoparticles catalyzed synthesis of 1,2,3-triazoles under solvent-free condition

Gangaprasad,Paul Raj,Kiranmye,Sasikala,Karthikeyan,Kutti Rani,Elangovan

supporting information, p. 3105 - 3108 (2016/07/06)

A regioselective and tunable synthesis of 1,5-disubstituted 1,2,3-triazloles from oxidative and eliminative [3+2] cycloadditions of nitroolefins and organic azides under solvent-free condition in the presence and absence of commercially available CuO nano

A general metal-free route towards the synthesis of 1,2,3-triazoles from readily available primary amines and ketones

Thomas, Joice,Jana, Sampad,John, Jubi,Liekens, Sandra,Dehaen, Wim

supporting information, p. 2885 - 2888 (2016/02/19)

An unprecedented approach that enables the direct and selective preparation of 1,5-disubstituted 1,2,3-triazoles from abundantly available building blocks such as primary amines, enolizable ketones and 4-nitrophenyl azide as a renewable source of dinitrogen via an organocascade process has been developed. Furthermore, this efficient methodology also enables the synthesis of fully functionalized and fused N-substituted heterocycles.

Designing 2-aminoimidazole alkaloids analogs with anti-biofilm activities: Structure-activities relationships of polysubstituted triazoles

Linares,Bottzeck,Pereira,Praud-Tabaris,Blache

experimental part, p. 6751 - 6755 (2011/12/21)

In order to discover novel probes that may help in the investigation and the control of bacterial biofilms, we have designed a library of triazole-based analogs of 2-aminoimidazole marine alkaloids: naamine A and isonaamine A. Twenty-two compounds were sc

Dipolar Cycloaddition Reactions of Organic Azides with some Acetylenic Compounds

Abu-Orabi, Sultan T.,Atfah, M. Adnan,Jibril, Ibrahim,Mari'i, Fakhri M.,Ali, Amer Al-Sheikh

, p. 1461 - 1468 (2007/10/02)

Phenyl azide 1 and several substituted benzyl azides 2a-o underwent 1,3-dipolar cycloaddition reactions with dimethyl acrtylenedicarboxylate 3, phenylacetylene 4 and ethyl propiolate 5 to afford the triazoles 6-13.The reactions of these azides with ethyl

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