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N,N'-(tetramethyl-p-phenylene)-bis-benzenesulfonamide is a complex organic compound with the molecular formula C22H26N2O4S2. It is a white crystalline solid that is soluble in water and various organic solvents. N,N'-(tetramethyl-p-phenylene)-bis-benzenesulfonamide is characterized by its symmetrical structure, featuring two benzenesulfonamide groups connected by a tetramethyl-p-phenylene bridge. It is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical properties. The compound's stability and reactivity can be influenced by the presence of the sulfonamide groups, which can form hydrogen bonds and participate in various chemical reactions. Its synthesis typically involves the reaction of tetramethyl-p-phenylene with benzenesulfonyl chloride, followed by a condensation reaction to form the final product.

19835-87-1

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19835-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19835-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19835-87:
(7*1)+(6*9)+(5*8)+(4*3)+(3*5)+(2*8)+(1*7)=151
151 % 10 = 1
So 19835-87-1 is a valid CAS Registry Number.

19835-87-1Relevant academic research and scientific papers

Synthesis and 13C NMR spectra of N-substituted p-quinonimines: III. N-arylthio- and N-arylsulfonyl-1,4-benzoquinonimines with enhanced electron-donor character of quinoid ring

Pirozhenko,Avdeenko,Yusina,Konovalova

, p. 1121 - 1128 (2007/10/03)

Incorporation of alkyl substituents into quinonimine fragments of N-arylthio- and N-arylsulfonyl-1,4-benzoquinonimines results in virtually equal changes in the chemical shifts of the carbon atoms from this fragment compared to those of unsubstituted and

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