212645-16-4

Basic information

• Product Name: 5-Phenylsulfanylethynyl-benzo[1,3]dioxole
• Synonyms: 5-Phenylsulfanylethynyl-benzo[1,3]dioxole
• CAS NO: 212645-16-4
• Molecular Weight: 254.309
• Mol File: 212645-16-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-Phenylsulfanylethynyl-benzo[1,3]dioxole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Phenylsulfanylethynyl-benzo[1,3]dioxole(212645-16-4)
• EPA Substance Registry System: 5-Phenylsulfanylethynyl-benzo[1,3]dioxole(212645-16-4)

Safety Data

• Hazardous Substances Data: 212645-16-4(Hazardous Substances Data)

Upstream product

• 92449-54-2 5-(2,2-dibromovinyl)-1,3-benzodioxol 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 212645-18-6 (CH₃CH₂CH₂CH₂)3Sn(SC₆H₅)CCHC₆H₃(O₂CH₂) 
• 212645-37-9 (3S,3aS,5S,6S,7aR)-3-Benzo[1,3]dioxol-5-yl-6-benzyloxy-5-methoxy-3a-phenylsulfanyl-octahydro-indole 
• 212645-39-1 C₂₃H₂₅NO₄S 
• 66164-58-7 5-((Z)-2-Phenylsulfanyl-vinyl)-benzo[1,3]dioxole 

Relevant articles and documents

Application of the 2-azaallyl anion cycloaddition method to an enantioselective total synthesis of (+)-coccinine

A highly functionalized perhydroindole is formed by the intramolecular [π4s+π2s] cycloaddition of a 2-azaallyl anion with a vinyl sulfide [Eq. (a)]. This is the key step in the total synthesis of (+)-coccinine, the enantiomer of the Amaryllidaceae alkaloi