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2-((3-(p-tolyl)prop-2-yn-1-yl)oxy)tetrahydro-2H-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

172264-70-9

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172264-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172264-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,2,6 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 172264-70:
(8*1)+(7*7)+(6*2)+(5*2)+(4*6)+(3*4)+(2*7)+(1*0)=129
129 % 10 = 9
So 172264-70-9 is a valid CAS Registry Number.

172264-70-9Relevant academic research and scientific papers

An efficient copper(I) complex catalyzed Sonogashira type cross-coupling of aryl halides with terminal alkynes

Thakur,Jaseer,Naidu, Ajay B.,Sekar, Govindasamy

, p. 2865 - 2869 (2009)

A wide range of arylated alkynes are synthesized from the corresponding aryl halides and terminal alkynes through Sonogashira type cross-coupling reactions through C(aryl)-C bond formation in the presence of a catalytic amount of N,N′-dibenzyl BINAM-CuI complex under mild reaction conditions.

Butenolide synthesis from functionalized cyclopropenones

Nguyen, Sean S.,Ferreira, Andrew J.,Long, Zane G.,Heiss, Tyler K.,Dorn, Robert S.,Row, R. David,Prescher, Jennifer A.

supporting information, p. 8695 - 8699 (2019/10/28)

A general method to synthesize substituted butenolides from hydroxymethylcyclopropenones is reported. Functionalized cyclopropenones undergo ring-opening reactions with catalytic amounts of phosphine, forming reactive ketene ylides. These intermediates can be trapped by pendant hydroxy groups to afford target butenolide scaffolds. The reaction proceeds efficiently in diverse solvents and with low catalyst loadings. Importantly, the cyclization is tolerant of a broad range of functional groups, yielding a variety of α- and γ-substituted butenolides.

Selectivity in Garratt-Braverman cyclization: An experimental and computational study

Maji, Manasi,Mallick, Dibyendu,Mondal, Sayantan,Anoop, Anakuthil,Bag, Subhendu Sekhar,Basak, Amit,Jemmis, Eluvathingal D.

supporting information; experimental part, p. 888 - 891 (2011/04/27)

Bispropargyl sulfones equipped with aromatic rings of dissimilar nature were synthesized. Under basic conditions, these sulfones isomerized to the bisallenic sulfones, creating a competitive scenario between two alternate Garratt-Braverman (GB) cyclizatio

Copper(I)-catalyzed Caryl-Calkynyl bond formation of aryl iodides with terminal alkynes

Thakur,Sekar

scheme or table, p. 2785 - 2789 (2010/01/21)

A wide range of internal alkynes are synthesized from the corresponding aryl iodides and terminal alkynes by Sonogashira-type cross-coupling reactions through Caryl-Calkynyl bond formation in the presence of a catalytic amount of readily available DBU-CuBr complex under mild reaction conditions. Georg Thieme Verlag Stuttgart.

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