119046-49-0

Basic information

• Product Name: (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol
• Synonyms: (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol
• CAS NO: 119046-49-0
• Molecular Weight: 250.413
• Mol File: 119046-49-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol(119046-49-0)
• EPA Substance Registry System: (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol(119046-49-0)

Safety Data

• Hazardous Substances Data: 119046-49-0(Hazardous Substances Data)

Upstream product

• 54655-07-1 lithium trimethylsilylacetylenide 
• 60656-87-3 benzyloxyacetoaldehyde 
• 14593-43-2 benzyl allyl ether 
• 119046-45-6 (+/-)-4-benzyloxy-3-hydroxy-1-trimethylsilyl-1-butyne 

Downstream Products

• 120505-34-2 (R)-3-Benzyloxy-2-methoxymethoxy-propionaldehyde 
• 120505-35-3 (R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde 
• 120505-33-1 (S)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde 
• 114826-56-1 ((S)-1-Benzyloxymethyl-allyloxy)-tert-butyl-dimethyl-silane 
• 78469-93-9 (2S,3R)-1-benzyloxy-3,4-epoxy-2-(1'-methoxy-1'-methylaethoxy)-butan 
• 120575-87-3 (R)-2-Benzyloxy-1-((2R,3R)-3-trimethylsilanyl-oxiranyl)-ethanol 
• 78469-92-8 (2R,3S)-1-benzyloxy-3,4-epoxy-2-(1'-methoxy-1'-methylaethoxy)-butan 
• 104863-52-7 (S)-3-Benzyloxy-2-methoxymethoxy-propionaldehyde 
• 114826-56-1 ((R)-1-Benzyloxymethyl-allyloxy)-tert-butyl-dimethyl-silane 
• 93553-66-3 (2R)-1-(benzyloxy)but-3-en-2-ol 
• 109613-59-4 (S)-1-(benzyloxy)but-3-en-2-ol 
• 119046-51-4 (2S,3S,4S)-1-O-benzyl-3,4-epoxy-4-(trimethylsilyl)butane-1,2-diol 
• 119180-87-9 (2S,3E)-1-(benzyloxy)-4-(trimethylsilyl)but-3-en-2-ol 

Relevant articles and documents

A HIGHLY EFFICIENT KINETIC RESOLUTION OF γ- AND β-TRIMETHYLSILYL SECONDARY ALLYLIC ALCOHOLS BY THE SHARPLESS ASYMMETRIC EPOXIDATION

Kinetic resolution of γ- and β-trimethylsilyl secondary allylic alcohols proceeds with very large and synthetically satisfactory rate differences for the two enentiomers, respectively, thus providing a convenient and widely applicable method for preparati