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N,N'-bi(methoxycarbonylmethyl)terphthalamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47233-57-8

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47233-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47233-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,2,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 47233-57:
(7*4)+(6*7)+(5*2)+(4*3)+(3*3)+(2*5)+(1*7)=118
118 % 10 = 8
So 47233-57-8 is a valid CAS Registry Number.

47233-57-8Relevant academic research and scientific papers

N,N′-bis(methoxycarbonylmethyl)-terephthalamide

Armelin, Elaine,Escudero, Encarnacion,Campos, Lourdes,Puiggali, Jordi

, p. 172 - 173 (2001)

Molecules of the title compound, dimethyl N,N′-(1,4-benzene-dicarboxamido)diacetate, C14H16N2O6, lie on inversion centres and are hydrogen bonded along a single direction that runs parallel to the crystallograph

Insight into hydrogen bonding of terephthalamides with amino acids: Synthesis, structural and spectroscopic investigations

Hachu?a, Barbara,Polasz, Anna,Ksi??ek, Maria,Kusz, Joachim,Kozik, Violetta,Matussek, Marek,Pisarski, Wojciech

, p. 2901 - 2912 (2017/04/26)

Several bis-terephthalamides based on methyl esters of amino acids including glycine (1), β-alanine (2), γ-aminobutyric acid (3) and ε-aminocaproic acid (4), X[sbnd](CH2)n[sbnd]HNOC[sbnd]C6H4[sbnd]CONH[sbnd](CH

Interpenetrated networks from a novel nanometer-sized pseudopeptidic ligand, bridging water, and transition metal ions with cds topology

Kostakis, George E.,Casella, Luigi,Hadjiliadis, Nick,Monzani, Enrico,Kourkoumelis, Nikolaos,Plakatouras, John C.

, p. 3859 - 3861 (2007/10/03)

The combination of a new pseudopeptidic ligand, transition metal ions, and bridging water molecules results in the formation of [M(μ-TBG)(μ-H 2O)(H2O)2] · 2H2O (M: Cu, Co and H2TBG: terephthaloylbisglycine); both compounds show rare two-fold interpenetrated three-dimensional cds-nets and reversible loss of coordinated and lattice water molecules. The Royal Society of Chemistry 2005.

A Convergent Synthesis of Carbohydrate-Containing Dendimers

Ashton, Peter R.,Boyd, Sue E.,Brown, Christopher L.,Jayaraman, Narayanaswamy,Nepogodiev, Sergey A.,Stoddart, J. Fraser

, p. 1115 - 1128 (2007/10/03)

The synthesis of carbohydrate-containing dendrimers has been achieved by a convergent grwoth approach.The synthetic strategy involves: 1) the synthesis of the triglucosylated derivative of tris(hydroxymethyl)methylamine (TRIS), 2) the introduction of a glycine-derived spacer and 3,3'-iminodipropionic acid derived branching units on to the TRIS derivative by amide bond formation, 3) condensation of the above saccharide-containing dendrons with a trifunctional 1,3,5-benzenetricarbonyl derivative, used as the core, by formation of amide bonds, and 4) deprotection of the saccharide units.A 9-mer and an 18-mer, carrying nine and eighteen saccharide units at the periphery, respectively, have been synthesized, in high yields at each step, by this synthetic strategy.By a variety of chromatographic and spectroscopic techniques, the dendrimers were shown to be structurally homogeneous, monodisperse, and error-free at all steps in their growth.These investigations were complemented by molecular modeling studies on the dendrimers.The presence of slightly distorted C3 symmetry was noted in both the 9-mer and the 18-mer. - Keywords: carbohydrates; cluster glucosides; convergent syntheses; dendrimers; neoglycoconjugates

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