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5,11,17,23-tetrakis(1,1-dimethylethyl)-25,26-bis(benzoyloxy)-27,28-bis(hydroxy)calix[4]arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

400642-08-2

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400642-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 400642-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 400642-08:
(8*4)+(7*0)+(6*0)+(5*6)+(4*4)+(3*2)+(2*0)+(1*8)=92
92 % 10 = 2
So 400642-08-2 is a valid CAS Registry Number.

400642-08-2Downstream Products

400642-08-2Relevant academic research and scientific papers

A fast access to non-symmetrically substituted 1,3-alternate conformers of calix[4]arenes

Kleij, Arjan W.,Prados, Pilar,De Mendoza, Javier

, p. 2848 - 2852 (2004)

A simple and direct protocol is reported for the synthesis of the first non-symmetrically substituted 1,3-alternate conformers of calix[4]arenes by selective mono-deacylation of a tribenzoyl precursor under basic conditions, followed by dialkylation. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Unexpected Single-Step Formation of 1,2-anti-Heterodisubstituted Calix[4]arenes upon Alkylation of a Tribenzoyl Precursor

Kleij, Arjan W.,Souto, Beatriz,Pastor, Cesar J.,Prados, Pilar,De Mendoza, Javier

, p. 8711 - 8714 (2007/10/03)

The selective preparation and complete structural characterization of a small series of 1,2-anti-hetero-disubstituted calix[4]arenes has been accomplished. These compounds were obtained in two steps from unsubstituted p-tert-butylcalix[4]arene by tribenzo

Synthesis and characterization of imidazole-substituted calix[4]arenes as simple enzyme-mimics with acyltransferase activity

Dospil, Günter,Schatz, Jürgen

, p. 7837 - 7840 (2007/10/03)

Calix[4]arenes which bear imidazole groups at different positions at the wide rim act as catalysts for enzyme-like release of p-nitrophenol from p-nitrophenyl esters in buffered solution.

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