441286-28-8

Basic information

• Product Name: (3R,4S,5S)-3-Benzyl-5-benzyloxymethyl-4-trimethylsilanyl-dihydro-furan-2-one
• Synonyms: (3R,4S,5S)-3-Benzyl-5-benzyloxymethyl-4-trimethylsilanyl-dihydro-furan-2-one
• CAS NO: 441286-28-8
• Molecular Weight: 368.548
• Mol File: 441286-28-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4S,5S)-3-Benzyl-5-benzyloxymethyl-4-trimethylsilanyl-dihydro-furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4S,5S)-3-Benzyl-5-benzyloxymethyl-4-trimethylsilanyl-dihydro-furan-2-one(441286-28-8)
• EPA Substance Registry System: (3R,4S,5S)-3-Benzyl-5-benzyloxymethyl-4-trimethylsilanyl-dihydro-furan-2-one(441286-28-8)

Safety Data

• Hazardous Substances Data: 441286-28-8(Hazardous Substances Data)

Upstream product

• 441286-20-0 Carbonic acid (1S,2S)-1-benzyloxymethyl-4-phenyl-2-trimethylsilanyl-but-3-ynyl ester ethyl ester 
• 441286-45-9 (2S,3S)-1-Benzyloxy-5-phenyl-3-trimethylsilanyl-pent-4-yn-2-ol 
• 138722-29-9 (2S,3S)-1-O-benzyl-2,3-epoxy-3-(trimethylsilyl)propane-1-ol 
• 5075-59-2 diethyl(phenylethynyl)aluminum 

Downstream Products

• 441286-32-4 (Z)-(S)-2-Benzyl-5-benzyloxy-pent-3-enoic acid 
• 68975-22-4 (R)-3-benzyltetrahydro-2H-pyran-2-one 

Relevant articles and documents

Asymmetric synthesis of stereodefined α-alkyl-γ-benzyloxymethyl-β-trimethylsilyl-γ- butyrolactones that serve as an efficient precursor for constructing carbon skeletons having a tertiary or quaternary stereogenic center

The optically active lactone 1 can be transformed to a chiral building block or intermediate for constructing carbon skeletons containing either a tertiary or quaternary stereogenic center by taking advantage of the steric bulk as well as the reactivity o