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(E)-1,4,7,10,13,16-Hexaoxa-cyclotetracos-20-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

601491-88-7

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601491-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 601491-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,1,4,9 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 601491-88:
(8*6)+(7*0)+(6*1)+(5*4)+(4*9)+(3*1)+(2*8)+(1*8)=137
137 % 10 = 7
So 601491-88-7 is a valid CAS Registry Number.

601491-88-7Upstream product

601491-88-7Downstream Products

601491-88-7Relevant academic research and scientific papers

Synthesis of a molecular charm bracelet via click cyclization and olefin metathesis clipping

Clark, Paul G.,Guidry, Erin N.,Chan, Wing Yan,Steinmetz, Wayne E.,Grubbs, Robert H.

, p. 3405 - 3412 (2010)

We describe the synthesis of a polycatenated cyclic polymer, a structure that resembles a molecular charm bracelet. Ruthenium-catalyzed ring-opening metathesis polymerization of an aminocontaining cyclic olefin monomer in the presence of a chain transfer agent generated an α,ω-diazide functionalized polyamine. Cyclization of the resulting linear polyamine using pseudo-high-dilution coppercatalyzed click cyclization produced a cyclic polymer in 19% yield. The click reaction was then further employed to remove linear contaminants from the cyclic polymer using azide- and alkyne-functionalized scavenging resins, and the purified cyclic polymer product was characterized by gel permeation chromatography, 1H NMR spectroscopy, and IR spectroscopy. Polymer hydrogenation and conversion to the corresponding polyammonium species enabled coordination and interlocking of diolefin polyether fragments around the cyclic polymer backbone using ruthenium-catalyzed ring-closing olefin metathesis to afford a molecular charm bracelet structure. This charm bracelet complex was characterized by 1H NMR spectroscopy, and the catenated nature of the small rings was confirmed using two-dimensional diffusionordered NMR spectroscopy.

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