99261-11-7

Basic information

• Product Name: (S)-3-Allyl-3-{(R)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-dihydro-furan-2-one
• CAS NO: 99261-11-7
• Molecular Weight: 438.609
• Mol File: 99261-11-7.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-Allyl-3-{(R)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-dihydro-furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-Allyl-3-{(R)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-dihydro-furan-2-one(99261-11-7)
• EPA Substance Registry System: (S)-3-Allyl-3-{(R)-1-[2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-ethyl}-dihydro-furan-2-one(99261-11-7)

Safety Data

• Hazardous Substances Data: 99261-11-7(Hazardous Substances Data)

Upstream product

• 21053-56-5 α-ethylidene-γ-butyrolactone 
• 72605-51-7 Lithiated 2-(3,4,5-trimethyloxyphenyl)-1,3-dithiane 
• 106-95-6 allyl bromide 

Relevant articles and documents

CONTROL ELEMENTS IN THE ASYMMETRIC TANDEM ALKYLATION OF α-ALKYLIDENE-γ-BUTYROLACTONE DERIVATIVES

Control elements in the highly selective construction of contiguous tertiary and quaternary carbon centers by the tandem alkylation of α-alkylidene-γ-butyrolactone derivatives were studied.It is clarified that the stereochemical course of the reaction is rationalized by evaluating highly selective 1,2-, 1,3-, and 1,4-asymmetric inductions.