1423165-85-8

Basic information

• Product Name: C₁₁H₁₉NO₃S
• Synonyms: C₁₁H₁₉NO₃S
• CAS NO: 1423165-85-8
• Molecular Weight: 245.343
• Mol File: 1423165-85-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₁H₁₉NO₃S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₁H₁₉NO₃S(1423165-85-8)
• EPA Substance Registry System: C₁₁H₁₉NO₃S(1423165-85-8)

Safety Data

• Hazardous Substances Data: 1423165-85-8(Hazardous Substances Data)

Upstream product

• 103-00-4 1-(cyclohexylamino)-2-propanol 
• 1423165-61-0 C₁₇H₃₅NO₃SSi 
• 1423165-69-8 C₁₁H₂₁NO₃S 
• 108-91-8 cyclohexylamine 

Downstream Products

• 1423165-93-8 2-cyclohexyl-4-methyl-5-methylene-1,1-dioxo-isothiazolidin-4-ol 
• 1423166-01-1 1-(2-cyclohexyl-1,1-dioxo-isothiazolidin-3-yl)-ethanone 

Relevant articles and documents

Syntheses of five- and seven-membered ring sultam derivatives by Michael addition and Baylis-Hillman reactions

Five- and seven-membered sultam derivatives were conveniently synthesized via intra- or intermolecular Michael additions and an improved vinyl sulfonamide Baylis-Hillman reaction. Two different cyclization pathways were explored for the oxa-Michael reaction. A good solvent was discovered for an otherwise sluggish ketone-type Baylis-Hillman reaction in which vinyl sulfonamide ketones were used as the precursors. Furthermore, a strong base caused vinyl sulfonamide ketones to undergo 5-endo-trig intramolecular cyclizations, which are disfavored according to Baldwin's rule. Finally Baylis-Hillman reaction products were used as scaffolds for diversity-oriented sultam syntheses.