944335-23-3

Basic information

• Product Name: (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate
• Synonyms: (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate
• CAS NO: 944335-23-3
• Molecular Weight: 426.533
• Mol File: 944335-23-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate(944335-23-3)
• EPA Substance Registry System: (2S)-4-[4-(benzyloxy)phenyl]-2-hydroxybutyl 4-methyl-1-benzenesulfonate(944335-23-3)

Safety Data

• Hazardous Substances Data: 944335-23-3(Hazardous Substances Data)

Upstream product

• 1638640-10-4 C₂₃H₂₅NO₃ 
• 69172-21-0 4-(4-Benzyloxyphenyl)butanal 
• 1166181-77-6 methyl 4-[4-(benzyloxy)phenyl]butanoate 
• 243641-03-4 C₁₈H₁₈O₃ 
• 944335-21-1 (4S)-4-[4-(benzyloxy)phenethyl]-2,2-dimethyl-1,3-dioxolane 
• 944335-20-0 4-{2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl}phenol 
• 944335-22-2 (2S)-4-[4-(benzyloxy)phenyl]butane-1,2-diol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 138948-80-8 (2R)-4-[4-(benzyloxy)phenyl]butan-2-ol 
• 59092-94-3 (R)-rhododendrol 
• 1010127-34-0 (2S)-2-{2-[4-(benzyloxy)phenyl]ethyl}oxirane 
• 1638640-04-6 ({(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-yl}oxy)(tert-butyl)(dimethyl)silane 
• 1638640-11-5 C₂₅H₃₆O₃Si 
• 1258516-47-0 {(1S)-3-[4-(benzyloxy)phenyl]-1-{[(2S)-oxiran-2-yl]methyl}propoxy}(tert-butyl)dimethylsilane 
• 1443256-45-8 (3S,5R)-1-(4-hydroxyphenyl)nonadecane-3,5-diol 

Relevant articles and documents

Asymmetric synthesis of (R)-(-)-rhododendrol, the aglycone of the hepatoprotective agent rhododendrin

Starting from 2,3-O-isopropylidene-D-glyceraldehyde (3) as chiral material, (R)-(-)-rhododendrol 2, the aglycone of the naturally occurring rhododendrin 1 was synthesized. Copyright Taylor & Francis Group, LLC.

An efficient approach to the stereoselective synthesis of 2,6-disubstituted dihydropyrans via stannyl-Prins cyclization

A general method has been developed for the stereoselective construction of 2,6-disubstituted dihydropyrans based on the Lewis acid-catalyzed intramolecular reactions of oxocarbenium ions with vinylstannanes. This novel methodology was applied to the enan