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5,11,17,23-tetra-tert-butyl-25,27-dihydroxy-26,28-bis(N-benzoyl-2-aminoethoxy)calix[4]arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353520-34-0

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353520-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353520-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,5,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 353520-34:
(8*3)+(7*5)+(6*3)+(5*5)+(4*2)+(3*0)+(2*3)+(1*4)=120
120 % 10 = 0
So 353520-34-0 is a valid CAS Registry Number.

353520-34-0Downstream Products

353520-34-0Relevant academic research and scientific papers

Choline esterase inhibitors and synthetic oxalic acid receptors based on calix[4]arene derivatives

Stoikov,Khrustalev,Ibragimova,Stoikova,Evtyugin,Antipin,Konovalov

, p. 278 - 284 (2005)

New reversible butyrylcholine esterase inhibitors based on calix[4]arene derivatives were suggested. A series of new distally disubstituted calix[4]arenes were prepared in 60-80% yields. Some of these compounds showed properties of reversible choline este

Synthetic receptors based on calix[4]arene functionalized at the lower rim in molecular recognition of dicarboxylic, α-hydroxycarboxylic, and α-amino acids

Stoikov,Gafiullina,Ibragimova,Antipin,Konovalov

, p. 1172 - 1180 (2007/10/03)

New calix[4]arenes, di- and tetrasubstituted at the lower rim, with different functional groups were synthesized. They were studied as carriers of a series of dicarboxylic and α-hydroxycarboxylic acids through a liquid impregnated membrane. The calix[4]arenes under study are capable of molecular recognition of oxalic acid in the series of structurally similar dicarboxylic and α-hydroxycarboxylic acids. The regularities found make it possible to change purposefully the receptor ability of 1,3-disubstituted calix[4]arenes by variation of the nature of substituents.

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