173097-12-6

Basic information

• Product Name: 2,3,5,5,6,6-Hexachloro-1,4-di-p-tolylsulfonylimino-2-cyclohexene
• Synonyms: 2,3,5,5,6,6-Hexachloro-1,4-di-p-tolylsulfonylimino-2-cyclohexene
• CAS NO: 173097-12-6
• Molecular Weight: 623.192
• Mol File: 173097-12-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,3,5,5,6,6-Hexachloro-1,4-di-p-tolylsulfonylimino-2-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5,5,6,6-Hexachloro-1,4-di-p-tolylsulfonylimino-2-cyclohexene(173097-12-6)
• EPA Substance Registry System: 2,3,5,5,6,6-Hexachloro-1,4-di-p-tolylsulfonylimino-2-cyclohexene(173097-12-6)

Safety Data

• Hazardous Substances Data: 173097-12-6(Hazardous Substances Data)

Upstream product

• 50931-32-3 N,N′-(cyclohexa-2,5-diene-1,4-diylidene)bis-(4-methylbenzenesulfonamide) 
• 41595-29-3 N,N'-ditosyl-p-phenylenediamine 
• 2654-77-5 N,N′-(cyclohexa-2,5-diene-1,4-diylidene)bis-(4-chlorobenzenesulfonamide) 
• 2654-68-4 4-chloro-N-(4-(((4-chlorophenyl)sulfonyl)amino)phenyl)benzenesulfonamide 
• 106-50-3 1,4-phenylenediamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 624-18-0 benzene-1,4-diamine hydrochloride 
• 98472-75-4 N,N'-bis-p-chlorobenzenesulfonyl-2-chloro-1,4-phenylenediamine 
• 76165-53-2 2,3,5,6-tetrachloro-N,N'-ditosyl-p-phenylenediamine 
• 76165-36-1 N,N'-bis-p-toluenesulfonyl-2,3,5,6-tetrachloro-1,4-benzoquinone diimine 

Downstream Products

• 118-75-2 chloranil 
• 14504-09-7 2,3,5,5,6,6-hexachloro-2-cyclohexene-1,4-dione 
• 76165-53-2 2,3,5,6-tetrachloro-N,N'-ditosyl-p-phenylenediamine 
• 134645-47-9 C₂₆H₂₉Cl₄N₂O₇PS₂ 

Relevant articles and documents

Reactions of Polyhalogenated 4-Arylsulfonylimino-2-cyclohexenones and 3,6-Bis(arylsulfonylimino)cyclohexenes with Alcohols

Polyhalogenated 4-arylsulfonylimino-2-cylohexenones and 3,6-bis(arylsulfonylimino)cyclohexenes react with alcohols to give 1,2-addition products at the C=N bond through intermediate formation of N-arylsulfonylimino-p-quinonimines. Heating of the adducts above the melting point results in elimination of alcohol molecule and formation of quinoid structures.