212645-39-1

Basic information

• Product Name: C₂₃H₂₅NO₄S
• Synonyms: C₂₃H₂₅NO₄S
• CAS NO: 212645-39-1
• Molecular Weight: 411.522
• Mol File: 212645-39-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₃H₂₅NO₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₂₅NO₄S(212645-39-1)
• EPA Substance Registry System: C₂₃H₂₅NO₄S(212645-39-1)

Safety Data

• Hazardous Substances Data: 212645-39-1(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 212645-37-9 (3S,3aS,5S,6S,7aR)-3-Benzo[1,3]dioxol-5-yl-6-benzyloxy-5-methoxy-3a-phenylsulfanyl-octahydro-indole 
• 212645-16-4 5-Phenylsulfanylethynyl-benzo[1,3]dioxole 
• 66164-58-7 5-((Z)-2-Phenylsulfanyl-vinyl)-benzo[1,3]dioxole 
• 212645-22-2 (E)-1-chloro-5-(4-methoxybenzyloxy)pent-2-ene 
• 201667-72-3 methyl (2E)-5-(4-methoxybenzyloxy)-2-pentenoate 
• 882-33-7 diphenyldisulfane 
• 158817-21-1 (E)-5-(4-methoxybenzyloxy)pent-2-en-1-ol 
• 92449-54-2 5-(2,2-dibromovinyl)-1,3-benzodioxol 

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