1258516-47-0

Basic information

• Product Name: {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane
• Synonyms: {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane
• CAS NO: 1258516-47-0
• Molecular Weight: 412.645
• Mol File: 1258516-47-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane(1258516-47-0)
• EPA Substance Registry System: {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane(1258516-47-0)

Safety Data

• Hazardous Substances Data: 1258516-47-0(Hazardous Substances Data)

Upstream product

• 1638640-11-5 C₂₅H₃₆O₃Si 
• 1638640-04-6 ({(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-yl}oxy)(tert-butyl)(dimethyl)silane 
• 767330-04-1 (-)-(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 
• 1010127-34-0 (2S)-2-{2-[4-(benzyloxy)phenyl]ethyl}oxirane 
• 944335-23-3 (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate 
• 944335-22-2 (2S)-4-[4-(benzyloxy)phenyl]butane-1,2-diol 
• 1638640-10-4 C₂₃H₂₅NO₃ 
• 69172-21-0 4-(4-Benzyloxyphenyl)butanal 
• 1166181-77-6 methyl 4-[4-(benzyloxy)phenyl]butanoate 
• 243641-03-4 C₁₈H₁₈O₃ 
• 1258516-46-9 (2S)-4-[4-(benzyloxy)phenyl]-1-[(2S)-oxiran-2-yl]butan-2-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 1187819-78-8 (4R,6S)-8-[4-(benzyloxy)phenyl]-6-{[(tert-butyl)dimethylsilyl]oxy}oct-1-en-4-ol 
• 1443256-45-8 (3S,5R)-1-(4-hydroxyphenyl)nonadecane-3,5-diol 

Relevant articles and documents

Stereoselective total synthesis of phenolic nonadecanediol

A simple and highly efficient synthetic route has been developed for synthesis of 1-(4-hydroxyphenyl)nonadecane-3,5-diol (1). The two stereogenic centers were generated by employing proline asymmetric α-hydroxylation (MacMillan α-hydroxylation), Jacobsen's hydrolytic kinetic resolution (HKR), and, finally, Yamaguchi oxirane opening as key steps (Scheme 2). Copyright