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ethyl (3,5-dioxo-1,2,4-dithiazolidin-4-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70711-36-3

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70711-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70711-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,1 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70711-36:
(7*7)+(6*0)+(5*7)+(4*1)+(3*1)+(2*3)+(1*6)=103
103 % 10 = 3
So 70711-36-3 is a valid CAS Registry Number.

70711-36-3Relevant academic research and scientific papers

A new and simple synthesis of sulfonyl ureas from sulfonamides and N-alkyl-1,2,4-dithiazolidine-3,5-diones

Gessner, Richard K.,Chibale, Kelly

experimental part, p. 2839 - 2843 (2010/03/03)

A new, short, and simple synthetic approach to sulfonyl ureas is reported. The method involves the transformation of readily synthesized N-alkyl-1,2,4-dithiazolidine-3,5-diones by reaction with primary sulfonamides. Sulfonyl ureas were obtained in moderat

Synthetic and structural studies on 1,2,4-dithiazolidine-3,5-dione derivatives

Wood, Mark E.,Cane-Honeysett, Daniel J.,Dowle, Michael D.,Coles, Simon J.,Hursthouse, Michael B.

, p. 3015 - 3023 (2007/10/03)

Methods have been developed for the N-alkylation of 1,2,4-dithiazolidine-3,5-dione 2 and the subsequent conversion of the N-alkylated derivatives into isocyanates 5. An extension of this methodology onto a solid-support is also reported. X-ray crystallographic analysis has been carried out on potassium 1,2,4-dithiazolidine-3,5-dione 3 for structural comparison with the parent heterocycle 2.

1,2,4-Dithiazolidine-3,5-dione: A nucleophilic isocyanate 'building block'

Cane-Honeysett,Dowle,Wood

, p. 1622 - 1624 (2007/10/03)

Mild conditions are described for the direct N-alkylation of 1,2,4-dithiazolidine-3,5-dione 1 using a variety of alkyl halides with subsequent conversion of the products 2 into alkyl isocyanates using triphenylphosphine.

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