6559-11-1

Basic information

• Product Name: 6-(octylsulfanyl)benzo[cd]indol-2(1H)-one
• CAS NO: 6559-11-1
• Molecular Formula: C₆H₁₂O₃
• Molecular Weight: 313.457
• Mol File: 6559-11-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 408.1°C at 760 mmHg
• Flash Point: 200.6°C
• Density: 1.16g/cm³
• Vapor Pressure: 7.2E-07mmHg at 25°C
• Refractive Index: 1.626
• CAS DataBase Reference: 6-(octylsulfanyl)benzo[cd]indol-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(octylsulfanyl)benzo[cd]indol-2(1H)-one(6559-11-1)
• EPA Substance Registry System: 6-(octylsulfanyl)benzo[cd]indol-2(1H)-one(6559-11-1)

Safety Data

• Hazardous Substances Data: 6559-11-1(Hazardous Substances Data)

Upstream product

• 86728-57-6 cis-3-<<(p-Nitrophenyl)sulfonyl>oxy>-2-methoxytetrahydropyran 
• 110-87-2 3,4-dihydro-2H-pyran 
• 67-56-1 methanol 
• 86728-74-7 2,3-dihydroxytetrahydropyran 

Downstream Products

• 86728-57-6 cis-3-<<(p-Nitrophenyl)sulfonyl>oxy>-2-methoxytetrahydropyran 

Relevant articles and documents

Epoxidation-alcoholysis of cyclic enol ethers catalyzed by Ti(O iPr)4 or Venturello's peroxophosphotungstate complex

Venturello's peroxophosphotungstate compound and Ti(OiPr) 4 were successfully used as catalysts for the epoxidation-alcoholysis of various dihydropyrans and dihydrofuran using H2O2 as the oxidant. Different alcohols can be used as solvents and nucleophiles, resulting in hydroxy ether products with varying alkoxy groups. The Venturello compound can also be used as catalyst in a biphasic conversion of dihydropyran, in which long chain alcohols or fatty acids are incorporated in the hydroxy ether products with high yield and (stereo)selectivity. This journal is The Royal Society of Chemistry.