159983-62-7

Basic information

• Product Name: C₁₈H₁₀Cl₆N₂O₄S₂
• Synonyms: C₁₈H₁₀Cl₆N₂O₄S₂
• CAS NO: 159983-62-7
• Molecular Weight: 595.138
• Mol File: 159983-62-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₀Cl₆N₂O₄S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₀Cl₆N₂O₄S₂(159983-62-7)
• EPA Substance Registry System: C₁₈H₁₀Cl₆N₂O₄S₂(159983-62-7)

Safety Data

• Hazardous Substances Data: 159983-62-7(Hazardous Substances Data)

Upstream product

• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 624-18-0 benzene-1,4-diamine hydrochloride 
• 173097-13-7 C₁₈H₈Cl₈N₂O₄S₂ 
• 2654-77-5 N,N′-(cyclohexa-2,5-diene-1,4-diylidene)bis-(4-chlorobenzenesulfonamide) 
• 98472-75-4 N,N'-bis-p-chlorobenzenesulfonyl-2-chloro-1,4-phenylenediamine 
• 2654-68-4 4-chloro-N-(4-(((4-chlorophenyl)sulfonyl)amino)phenyl)benzenesulfonamide 

Downstream Products

• 173097-13-7 C₁₈H₈Cl₈N₂O₄S₂ 
• 159983-63-8 C₁₈H₈Cl₆N₂O₄S₂ 

Relevant articles and documents

Some Reactions of 3,6-Bis(arylsulfonylimino)-1,2,4,4,5,5-hexachlorocyclohexenes

Reduction of 3,6-bis(arylsulfonylimino)-1,2,4,4,5,5-hexachlorocyclohexenes with Zn in CH3COOH or Na2S2O4 results in elimination of two chlorine atoms to give a benzoid structure.A similar effect is produced by dialkyl hydrogen phosphites.Reactions of the title compounds with methanol and primary aromatic amines result in 1,2-addition.Treatment with secondary amines leads to nucleophilic substitution of chlorine at the sp2-hybridized carbon atom.Reactions with trimethylsilyl dialkyl phosphites proceed in two directions: elimination of two chlorine atoms and 1,6-addition followed by hydrolysis of the intermediate adduct.