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N-{(E)-[methyl(phenyl)amino]methylidene}methanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78523-05-4

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78523-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78523-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,2 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78523-05:
(7*7)+(6*8)+(5*5)+(4*2)+(3*3)+(2*0)+(1*5)=144
144 % 10 = 4
So 78523-05-4 is a valid CAS Registry Number.

78523-05-4Downstream Products

78523-05-4Relevant academic research and scientific papers

Improved synthesis of N-sulfonylformamidine derivatives promoted by thionyl chloride

Hudabaierdi, Ruzeahong,Wusiman, Abudureheman,Mulati, Ayinigeer

, p. 485 - 489 (2017)

An improved synthesis of N-sulfonylformamidine derivatives has been developed involving direct condensation of various sulfonamides and formamides in the presence of thionyl chloride using chloroform as solvent. Detailed synthetic studies indicate that th

In situ formation of vilsmeier reagents mediated by oxalyl chloride: A tool for the selective synthesis of N-sulfonylformamidines

Gazvoda, Martin,Kocevar, Marijan,Polanc, Slovenko

supporting information, p. 5381 - 5386 (2013/09/02)

N-Sulfonylformamidines were produced from sulfonamides or N-acylated sulfonamides using Vilsmeier reagent obtained in situ from N,N-disubstituted formamides and oxalyl chloride. Optically active substrates did not racemize during the process. The efficient and mild cleavage of N-sulfonylformamidines can be achieved with hydrazine hydrate in ethanol. The entire procedure constitutes a simple method for protecting, and deprotecting, the sulfonamide moiety. A straightforward and efficient synthesis for N-sulfonylformamidines by employment of various Vilsmeier reagents generated in situ is described. The reactions proceed under mild reaction conditions and tolerate several sensitive functional groups. Copyright

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