41772-29-6

Basic information

• Product Name: Benzenesulfenamide, N-(3,5-dimethyl-4-oxo-2,5-cyclohexadien-1-ylidene)-
• CAS NO: 41772-29-6
• Molecular Formula: C14H13NOS
• Molecular Weight: 243.329
• Mol File: 41772-29-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfenamide, N-(3,5-dimethyl-4-oxo-2,5-cyclohexadien-1-ylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfenamide, N-(3,5-dimethyl-4-oxo-2,5-cyclohexadien-1-ylidene)-(41772-29-6)
• EPA Substance Registry System: Benzenesulfenamide, N-(3,5-dimethyl-4-oxo-2,5-cyclohexadien-1-ylidene)-(41772-29-6)

Safety Data

• Hazardous Substances Data: 41772-29-6(Hazardous Substances Data)

Upstream product

• 576-26-1 2.6-dimethylphenol 
• 41772-19-4 Triphenylsulfenamid 
• 5184-27-0 C₁₂H₁₀ClNO₂S₂ 
• 15980-22-0 3,5-dimethyl-4-hydroxyaniline 
• 4972-29-6 benzenesulphinyl chloride 
• 24364-84-9 bis-benzenesulfenyl-amine 
• 931-59-9 benzenesulfenyl chloride 
• 527-60-6 Mesitol 

Relevant articles and documents

Comparison of preparation methods of N-arylsulfinyl-1,4-benzoquinone monoimines

Advantages and shortcomings were discussed of three procedures for preparation N-arylsulfinyl-1,4-benzoquinone imines: the reaction of arenesulfenyl chlorides with 1,4-benzoquinone oximes, the oxidation of N-arylthio-1,4-benzoquinone imines, and the reaction of arylsulfinyl chlorides with p-aminophenols followed by oxidation. A series of new N-arylsulfinyl-1,4- benzoquinone imines was obtained.

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

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