222023-27-0

Basic information

• Product Name: 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone
• Synonyms: 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone
• CAS NO: 222023-27-0
• Molecular Weight: 356.529
• Mol File: 222023-27-0.mol

Chemical Properties

• CAS DataBase Reference: 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone(222023-27-0)
• EPA Substance Registry System: 3-Isobutoxy-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enone(222023-27-0)

Safety Data

• Hazardous Substances Data: 222023-27-0(Hazardous Substances Data)

Upstream product

• 123289-30-5 1-(Phenylthio)-1-(trimethylsilyl)-1,2-propadiene 
• 222023-26-9 3-(4-isobutoxy-2-oxo-cyclohexen-3-enyl)-propionaldehyde 
• 23074-59-1 3-isobutoxycyclohex-2-en-1-one 
• 223103-61-5 6-(3-hydroxy-propyl)-3-isobutoxy-2-cyclohexen-1-one 
• 223103-60-4 6-<3-(tert-butyldimethylsilyloxy)-propyl>-3-isobutoxy-2-cyclohexen-1-one 

Downstream Products

• 222023-21-4 3-Isobutoxy-1-methyl-6-((Z)-4-phenylsulfanyl-hexa-3,5-dienyl)-cyclohex-2-enol 

Relevant articles and documents

Functionalized carbocyclic rings via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media

The synthesis of highly structured carbocyclic ring systems possessing quaternary carbon atoms has been realized via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media.