2973-83-3

Basic information

• Product Name: Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester
• CAS NO: 2973-83-3
• Molecular Formula: C9H10ClNO2S2
• Molecular Weight: 263.769
• Mol File: 2973-83-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester(2973-83-3)
• EPA Substance Registry System: Carbonochloridimidothioic acid, [(4-methylphenyl)sulfonyl]-, methyl ester(2973-83-3)

Safety Data

• Hazardous Substances Data: 2973-83-3(Hazardous Substances Data)

Upstream product

• 2651-15-2 N-[bis(methylthio)methylene]-p-toluenesulfonamide 

Downstream Products

• 65159-17-3 N-(toluene-4-sulfonyl)-morpholine-4-carboximidothioic acid methyl ester 
• 5667-49-2 N--O-benzyl-hydroxylamin 
• 145198-65-8 N-[1-sec-Butylamino-1-methylsulfanyl-meth-(E)-ylidene]-4-methyl-benzenesulfonamide 
• 138761-14-5 C₂₀H₂₉N₃O₃S₃ 
• 138761-12-3 C₂₁H₂₅N₃O₂S₃ 
• 81261-46-3 methyl-N-hexyl-N'-toluenesulfonylcarbonimidodithioate 
• 81261-48-5 N-[1-Heptylamino-1-methylsulfanyl-meth-(Z)-ylidene]-4-methyl-benzenesulfonamide 
• 81261-50-9 N-[1-Decylamino-1-methylsulfanyl-meth-(Z)-ylidene]-4-methyl-benzenesulfonamide 
• 81261-45-2 4-Methyl-N-[1-methylsulfanyl-1-pentylamino-meth-(Z)-ylidene]-benzenesulfonamide 
• 120563-91-9 N-[1-tert-Butylamino-1-methylsulfanyl-meth-(Z)-ylidene]-4-methyl-benzenesulfonamide 
• 10219-51-9 N,N'-Dibutyl-N''-tosyl-guanidin 
• 81261-42-9 N-[1-Allylamino-1-methylsulfanyl-meth-(Z)-ylidene]-4-methyl-benzenesulfonamide 

Relevant articles and documents

Synthesis of Cyclic Guanidines Bearing N-Arylsulfonyl and N-Cyano Protecting Groups via Pd-Catalyzed Alkene Carboamination Reactions

Palladium-catalyzed carboamination reactions of N-allylguanidines bearing cleavable N-cyano or N-arylsulfonyl protecting groups are described. The reactions afford cyclic guanidine products in good yield, and transformations of substrates bearing internal alkenes proceed with high diastereoselectivity. Deuterium labeling studies indicate these transformations proceed via anti-aminopalladation pathways.

Synthesis of Cyclic Guanidines via Silver-Catalyzed Intramolecular Alkene Hydroamination Reactions of N-Allylguanidines

The silver-catalyzed hydroamination of tosyl-protected N-allylguanidines is described. These reactions provide substituted cyclic guanidines in high yields. The reactions are amenable to the construction of quaternary stereocenters as well as both monocyc

Routes to functionalized guanidines. The synthesis of guanidino diesters.

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