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1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849052-75-1

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849052-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849052-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849052-75:
(8*8)+(7*4)+(6*9)+(5*0)+(4*5)+(3*2)+(2*7)+(1*5)=191
191 % 10 = 1
So 849052-75-1 is a valid CAS Registry Number.

849052-75-1Downstream Products

849052-75-1Relevant academic research and scientific papers

Anion-templated assembly of pseudorotaxanes: Importance of anion template, strength of ion-pair thread association, and macrocycle ring size

Sambrook, Mark R.,Beer, Paul D.,Wisner, James A.,Paul, Rowena L.,Cowley, Andrew R.,Szemes, Fridrich,Drew, Michael G. B.

, p. 2292 - 2302 (2005)

A wide range of pseudorotaxane assemblies containing positively charged pyridinium, pyridinium nicotinamide, imidazolium, benzimidazolium and guanidinium threading components, and macrocyclic isophthalamide polyether ligands have been prepared using a general anion templation procedure. In noncompetitive solvent media, coupling halide anion recognition by a macrocyclic ligand with ion-pairing between the halide anion and a strongly associated cation provides the driving force for interpenetration. Extensive solution 1H NMR binding studies, thermodynamic investigations, and single-crystal X-ray structure determinations reveal that the nature of the halide anion template, strength of the ion-pairing between the anion template and the cationic threading component, and to a lesser extent favorable second sphere π-π aromatic stacking interactions between the positively charged threading component and macrocyclic ligand, together with macrocyclic ring size, affect the efficacy of pseudorotaxane formation.

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