206008-10-8

Basic information

• Product Name: CH₃OSn(CH₃)2S(NSO₂C₆H₄Cl)Sn(CH₃)2SSn(CH₃)2NHSO₂C₆H₄Cl
• Synonyms: CH₃OSn(CH₃)2S(NSO₂C₆H₄Cl)Sn(CH₃)2SSn(CH₃)2NHSO₂C₆H₄Cl
• CAS NO: 206008-10-8
• Molecular Weight: 921.758
• Mol File: 206008-10-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: CH₃OSn(CH₃)2S(NSO₂C₆H₄Cl)Sn(CH₃)2SSn(CH₃)2NHSO₂C₆H₄Cl(CAS DataBase Reference)
• NIST Chemistry Reference: CH₃OSn(CH₃)2S(NSO₂C₆H₄Cl)Sn(CH₃)2SSn(CH₃)2NHSO₂C₆H₄Cl(206008-10-8)
• EPA Substance Registry System: CH₃OSn(CH₃)2S(NSO₂C₆H₄Cl)Sn(CH₃)2SSn(CH₃)2NHSO₂C₆H₄Cl(206008-10-8)

Safety Data

• Hazardous Substances Data: 206008-10-8(Hazardous Substances Data)

Upstream product

• 16892-64-1 2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-trithiatristanninane 
• 30066-82-1 N-chloro-p-chlorobenzenesulfonamide sodium salt 

Downstream Products

• 98-64-6 4-Chlorobenzenesulfonamide 
• 206008-12-0 hydroxydimethyltin sulfite 
• 206008-11-9 hydroxydimethyltin sulfate 
• 16892-64-1 2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-trithiatristanninane 

Relevant articles and documents

Reaction of Trimeric Dimethyltin Sulfide with Sodium 4,N-Dichlorobenzenesulfamidate

Reaction of the trimeric cyclic dimethyltin sulfide (Me2SnS)3 with sodium 4,N-dichlorobenzenesulfamidate (Khloramin-KhB) at a 1:2 molar ratio in anhydrous methanol first results in clevage of the six-membered ring with Khloramin-KhB and release of one of the three sulfur atoms in the form of S0 (oxidative degradation). The second stage involves oxidative imination of one of the two remaining sulfur atoms in the resulting acyclic compound with a second Khloramin-KhB molecule to give organotin sufimide, including a -Me2SnS(=NSO2C6H4Cl 4)SnMe2- functional fragment. Hydrolysis of this sulfimide gives 4-chlorobenzenesulfamide and the sulfite HO-Me2Sn-O-S(=O)-O-SnMe2-OH.