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35274-21-6

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35274-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35274-21-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35274-21:
(7*3)+(6*5)+(5*2)+(4*7)+(3*4)+(2*2)+(1*1)=106
106 % 10 = 6
So 35274-21-6 is a valid CAS Registry Number.

35274-21-6Relevant academic research and scientific papers

Catalyst- and Supporting-Electrolyte-Free Electrosynthesis of Benzothiazoles and Thiazolopyridines in Continuous Flow

Folgueiras-Amador, Ana A.,Qian, Xiang-Yang,Xu, Hai-Chao,Wirth, Thomas

supporting information, p. 487 - 491 (2017/12/15)

A catalyst- and supporting electrolyte-free method for electrochemical dehydrogenative C?S bond formation in continuous flow has been developed. A broad range of N-arylthioamides have been converted to the corresponding benzothiazoles in good to excellent yields and with high current efficiencies. This transformation is achieved using only electricity and laboratory grade solvent, avoiding degassing or the use of inert atmosphere. This work highlights three advantages of electrochemistry in flow, which is (i) a supporting electrolyte-free reaction, (ii) an easy scale-up of the reaction without the need for a larger reactor and, (iii) the important and effective impact of having a good mixing of the reaction mixture, which can be achieved effectively with the use of flow systems. This clearly improves the reported methods for the synthesis of benzothiazoles.

A convenient synthesis of β-lactams from alkylthioimidates

Grochowski, Edward,Pupek, Krzysztof

, p. 6759 - 6768 (2007/10/02)

Stereoselective syntheses of trans-3,4,4-substituted-azetidin-2-ones from alkylthioimidates are described. Reduction of these compounds gave stereoselectively cis-4-alkyl-azetidin-2-ones which could be useful intermediates for preparation of biologically

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