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trans-1-acetamido-2-benzylthiocyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77134-93-1

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77134-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77134-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,3 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77134-93:
(7*7)+(6*7)+(5*1)+(4*3)+(3*4)+(2*9)+(1*3)=141
141 % 10 = 1
So 77134-93-1 is a valid CAS Registry Number.

77134-93-1Relevant academic research and scientific papers

Anodic Acetamidosulphenylation of Alkenes via Anodic Oxidation of Disulphides

Bewick, Alan,Coe, David E.,Mellor, John M.,Owton, W. Martin

, p. 1033 - 1038 (2007/10/02)

Anodic oxidation, at platinum and carbon electrodes, of dimethyl, diphenyl, dibenzyl, and heterocyclic disulphides in acetonitrile in the presence of alkenes affords products of acetamidosulphenylation.With cyclic alkenes a high selectivity for trans-addi

Additions to Alkenes via Metal Ion-Promoted Oxidation of Dialkyl and Diaryl Disulphides

Bewick, Alan,Mellor, John M.,Owton, W. Martin

, p. 1039 - 1044 (2007/10/02)

Reactions of alkenes with di-n-propyl, diphenyl, and dibenzyl disulphide in the presence of lead(IV) salts in trifluoroacetic acid-dichloromethane are described.The products, vicinal trifluoroacetoxysulphides, are obtained in higher yields with manganese(III) salts as the oxidant.Alternative reaction conditions with use of iron(III) salts or in the absence of added metal salts are also described.Trifluoroacetoxysulphides derived from diphenyl disulphide react with acetonitrile under Ritter conditions to give acetamidosulphides but trifluoroacetoxysulphides derived from dibenzyl disulphide only give the vicinal acetamidosulphides in poor yield as a result of an alternative reaction pathway affording benzylacetamide.Conversions of acetamidosulphides into aminosulphides and into acetamidothiols are described.

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