155099-15-3

Basic information

• Product Name: 2,2-Dibenzyl-3-<(tert-butyldimethylsilyl)oxy>-1-propanol
• CAS NO: 155099-15-3
• Molecular Weight: 370.607
• Mol File: 155099-15-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,2-Dibenzyl-3-<(tert-butyldimethylsilyl)oxy>-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dibenzyl-3-<(tert-butyldimethylsilyl)oxy>-1-propanol(155099-15-3)
• EPA Substance Registry System: 2,2-Dibenzyl-3-<(tert-butyldimethylsilyl)oxy>-1-propanol(155099-15-3)

Safety Data

• Hazardous Substances Data: 155099-15-3(Hazardous Substances Data)

Upstream product

• 31952-16-6 2,2-dibenzyl-1,3-propanediol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 72013-65-1 Dimethyl 2,2-dibenzylmalonate 
• 100-39-0 benzyl bromide 

Downstream Products

• 146903-01-7 (S)-2,2-Dibenzyl-5-<(tert-butoxycarbonyl)amino>-6-phenyl-(E)-3-hexen-1-ol 
• 146903-02-8 (S)-2,2-Dibenzyl-5-<(tert-butoxycarbonyl)amino>-6-phenyl-(E)-3-hexenoic acid 
• 155099-10-8 Methyl (S)-2,2-dibenzyl-5-<(tert-butoxycarbonyl)amino>-6-phenyl-(E)-3-hexenoate 
• 146902-98-9 2,2-Dibenzyl-3-<(tert-butyldimethylsilyl)oxy>propanal 

Relevant articles and documents

Stereoselective Epoxidation of Phe-Gly and Phe-Phe Vinyl Isosteres

Novel Phe-Gly and Phe-Phe isosteres have been synthesized.Vinylic isosteres of Phe-Gly and Phe-Phe were prepared by facile Julia reactions, and the resulting stereoisomers were isolated and epoxidized (m-chloroperbenzoic acid).Observed stereoselectivities