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N2C12H6(C6H4(OCH2CH2)3OCH2CCH)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1064652-53-4

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1064652-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1064652-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,4,6,5 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1064652-53:
(9*1)+(8*0)+(7*6)+(6*4)+(5*6)+(4*5)+(3*2)+(2*5)+(1*3)=144
144 % 10 = 4
So 1064652-53-4 is a valid CAS Registry Number.

1064652-53-4Relevant academic research and scientific papers

"Click" methodology for synthesis of functionalized [3]catenanes: Toward higher interlocked structures

Megiatto Jr., Jackson D.,Schuster, David I.

, p. 5444 - 5448 (2009)

A study was conducted to demonstrate the use of 'click' methodology for synthesizing higher interlocked structures of functionalized [3]catenanes. The strategy was based on the separate threading of two phenanthroline string-like fragments, containing ter

Optimizing reaction conditions for synthesis of electron donor-[60]fullerene interlocked multiring systems

Megiatto Jr., Jackson D.,Spencer, Robert,Schuster, David I.

supporting information; experimental part, p. 1544 - 1550 (2011/10/05)

Reaction conditions have been developed for the preparation of a series of rotaxanes and catenanes with appended electron-donor and electron-acceptor ([60]fullerene) subunits using a straightforward one-pot procedure based on Cu(i)-template synthesis and

Introduction of useful peripheral functional groups on [2]catenanes by combining Cu(i) template synthesis with click chemistry

Megiatto Jr., Jackson D.,Schuster, David I.

experimental part, p. 276 - 286 (2010/06/14)

Two protocols based on Cu(i) template synthesis and click reactions for the synthesis of functionalized [2]catenanes are described. A straightforward procedure, involving high dilution conditions at high temperatures (70 °C), affords [2]catenanes bearing two identical peripheral groups in high yields. For the preparation of non-symmetrically functionalized [2]catenanes, a second milder and simpler protocol was developed, generalizing and extending the method. The introduction of peripheral functional groups into the catenane structure opens up possibilities of using [2]catenanes as building blocks for preparation of even more complex structures.

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