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(RS)-biphenyl-2,2',6,6'-tetracarboxylic acid 2,2'-dibenzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

206647-29-2

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206647-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206647-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,6,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 206647-29:
(8*2)+(7*0)+(6*6)+(5*6)+(4*4)+(3*7)+(2*2)+(1*9)=132
132 % 10 = 2
So 206647-29-2 is a valid CAS Registry Number.

206647-29-2Relevant academic research and scientific papers

Self-assembly of enantiopure and racemic 2,2′,6,6′-tetrasubstituted biaryl tectons into hydrogen bonded chiral squares and infinite chiral square layers

Holy, Petr,Zavada, Jiri,Cisarova, Ivana,Podlaha, Jaroslav

, p. 3035 - 3045 (2007/10/03)

Both chiral and achiral hydrogen bonding o-,o-,o′-,o′-tetrasubstituted biaryls often exhibit unique self-assembling properties giving rise to chiral square cyclotetramers. The individual chiral squares self-assemble further with the formation of infinite layers which are either achiral or are chiral (homochiral). A priori analysis reveals various hydrogen bonding modes which may take part in the self-assembly, differing each from the other by structure and symmetry of the resulting squares and layers. Results of the theoretical analysis are compared with the experimental findings obtained from X-ray crystallographic analysis of three novel and two already known isosteric biaryl tectons, (S)-2a, (RS)-2a, 3a, (S)-5 and (RS)-5, respectively.

The activated core approach to combinatorial chemistry: A selection of new core molecules

Pryor, Kent E.,Shipps Jr., Gerald W.,Skyler, David A.,Rebek Jr., Julius

, p. 4107 - 4124 (2007/10/03)

Four new activated core molecules suitable for use in solution-phase combinatorial organic chemistry have been prepared. These molecules represent an attempt to further explore shape-space and increase the structural diversity of prepared libraries, as well as to incorporate recognition elements in the cores to increase the chances for interaction with biological targets. Demonstrations of deconvolution strategies used to simplify complex libraries and build individual molecular species based on the cores are also provided.

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