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Benzene, 1,2-bis[[2-[2-(2-chloroethoxy)ethoxy]ethyl]seleno]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136755-50-5

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136755-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136755-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136755-50:
(8*1)+(7*3)+(6*6)+(5*7)+(4*5)+(3*5)+(2*5)+(1*0)=145
145 % 10 = 5
So 136755-50-5 is a valid CAS Registry Number.

136755-50-5Downstream Products

136755-50-5Relevant academic research and scientific papers

Tetraselena crown ethers: Synthesis and complexation with mercury salts. Crystal structure of a macrocycle and a mercury(II) complex

Mazouz, Ahmed,Meunier, Philippe,Kubicki, Marek M.,Hanquet, Bernard,Amardeil, Regine,Bornet, Celine,Zahidi, Assou

, p. 1043 - 1048 (2007/10/03)

Dipotassium benzene-1,2-diselenolate, C6H4(SeK)2-1,2 obtained from the reaction of potassium tert-butoxide with a (benzene-1,2-diselenolato)zirconocene, was treated with C6H4[SeCH2(CH2OCH2) nCH2X]2-1,2 (X = Cl, n = 1 1, n = 2 2, n = 3 3 or X = Br n = 3 4) leading to tetraselenacrown ethers C6H4[SeCH2(CH2OCH2) nCH2Se]2-C6H4 (n = 1 6, n = 2 7 or n = 3 8) in a moderate yield (10-20%). This yield can be increased by using the 'caesium effect' from benzene-1,2-diselenol (18-40%). These macrocyclic compounds are able to complex heavy metals [especially mercury(II) ions] via their selenium atoms. The mercury complexes have been characterized by multinuclear NMR spectroscopy. The molecular structures of the tetraselenacrown ether 7 and the mercury complex of macrocycle 8 have been established by X-ray diffraction.

SYNTHESIS OF SELENIUM-CONTAINING CROWN ETHERS AND RELATED COMPOUNDS

Mazouz, Ahmed,Bodiguel, Jacques,Meunier, Philippe,Gautheron, Bernard

, p. 247 - 249 (2007/10/02)

The synthesis of the first examples of selenium-containing crown ethers from the benzene diselenolate anion and dichalcogenated ethers is reported.The reaction is highly dependent on the experimental conditions, particularly the concentration. 1H NMR and mass spectrometry were used to confirm the structures of the new compounds. Keywords: Benzene diseleno crown ethers; benzene diselenopolyethers; 1H NMR

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