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210780-05-5

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210780-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210780-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,7,8 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210780-05:
(8*2)+(7*1)+(6*0)+(5*7)+(4*8)+(3*0)+(2*0)+(1*5)=95
95 % 10 = 5
So 210780-05-5 is a valid CAS Registry Number.

210780-05-5Relevant articles and documents

Syntheses, reactions and crystal structures of 1,3-alternate p-tert-butylthiacalix[4]arene esters and amides

Liu, Li,Huang, Kun,Yan, Chao Guo

, p. 349 - 355 (2010)

p-tert-Butylthiacalix[4]arene was efficiently alkylated in the system of K2CO3/KI/acetone to give several thiacalixarene derivatives in 1,3-alternate conformation with functional ester, chloro, cyano and amide groups. Thiacalixarene tetraacateate can be converted to bicyclic amides by ammonolysis with alkylenediamine, and to sulfonylcalixarene by oxidation with hydrogen peroxide in acetic acid. Single crystal X-ray diffraction analysis reveals that thiacalixarene and sulfonylcalixarene exist mainly in 1,3-alternate conformation.

Synthesis of multivalent oxamate ligands based on calix[4]arene and thiacalix[4]arene backbones in 1,3-Alternate conformation

Noamane, Mohamed Habib,Ferlay, Sylvie,Abidi, Rym,Hosseini, Mir Wais

, p. 4259 - 4264 (2017/07/03)

Five new multivalent ligands based on either p-tert-butylthiacalix[4]arene (TCA) 1 or p-tert-butylcalix[4]arene (CA) 2 backbones in 1,3-Alternate conformation bearing four oxamate coordinating groups at their lower rim were designed and synthesized by a multistep strategy. These ligands differ either by the nature of the calix[4]arene backbone (CA or TCA) or by the nature of the spacer ((CH2)n) connecting the oxamate binding units to the backbone.

Synthesis and aggregation properties of thiacalix[4]arene tetra-N-acylamides

Kleshnina,Fi Long,Solov'eva,Antipin,Konovalov

, p. 430 - 435 (2015/05/04)

First 1,3-alternate p-tert-butylthiacalix[4]arenes containing N-acylamide fragments have been synthesized by reaction of thiacalix[4]arene carboxylic acid chlorides with 2-substituted 4,5-dihydro-1,3-oxazoles, and their aggregation properties have been st

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