1643935-92-5

Basic information

• Product Name: phenyl (S)-3-hydroxy-4-(3-hydroxypropyl)-1-methyl-5-methylene-2-oxocyclopent-3-ene-1-carboxylate
• CAS NO: 1643935-92-5
• Molecular Weight: 302.327
• Mol File: 1643935-92-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: phenyl (S)-3-hydroxy-4-(3-hydroxypropyl)-1-methyl-5-methylene-2-oxocyclopent-3-ene-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl (S)-3-hydroxy-4-(3-hydroxypropyl)-1-methyl-5-methylene-2-oxocyclopent-3-ene-1-carboxylate(1643935-92-5)
• EPA Substance Registry System: phenyl (S)-3-hydroxy-4-(3-hydroxypropyl)-1-methyl-5-methylene-2-oxocyclopent-3-ene-1-carboxylate(1643935-92-5)

Safety Data

• Hazardous Substances Data: 1643935-92-5(Hazardous Substances Data)

Upstream product

• 10226-28-5 ethyl 6-methyl-3,4-dihydro-2H-pyran-5-carboxylate 
• 5399-21-3 6-methyl-3,4-dihydro-2H-pyran-5-carboxylic acid 
• 1643935-77-6 (E)-phenyl 3-(benzhydryloxy)-2-methyl-4-(6-methyl-3,4-dihydro-2H-pyran-5-yl)-4-oxobut-2-enoate 
• 41717-27-5 C₇H₉ClO₂ 
• 1643935-61-8 (E)-phenyl 3-(benzhydryloxy)-2-methylacrylate 

Relevant articles and documents

Catalytic enantioselective nazarov cyclization: Construction of vicinal all-carbon-atom quaternary stereocenters

The diastereoselective asymmetric synthesis of vicinal all-carbon-atom quaternary stereocenters is a challenging problem in organic synthesis for which only few solutions have been described. A catalytic asymmetric Nazarov cyclization of fully substituted dienones that provides cyclopentenone derivatives with vicinal quaternary stereocenters in high optical purity and as single diastereoisomers is now reported.