128854-60-4

Basic information

• Product Name: (S)-methyl mandelyl tetrahydropyranyl ether
• Synonyms: (S)-methyl mandelyl tetrahydropyranyl ether
• CAS NO: 128854-60-4
• Molecular Weight: 250.295
• Mol File: 128854-60-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-methyl mandelyl tetrahydropyranyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl mandelyl tetrahydropyranyl ether(128854-60-4)
• EPA Substance Registry System: (S)-methyl mandelyl tetrahydropyranyl ether(128854-60-4)

Safety Data

• Hazardous Substances Data: 128854-60-4(Hazardous Substances Data)

Upstream product

• 17199-29-0 (S)-Mandelic acid 
• 110-87-2 3,4-dihydro-2H-pyran 
• 21210-43-5 (S)-Methyl mandelate 
• 611-71-2 (R)-Mandelic Acid 
• 20698-91-3 (R)-methyl mandelate 

Downstream Products

• 105769-50-4 (R)-(+)-2-chloro-2-phenylethyl p-chlorophenyl sulfone 
• 105769-48-0 (R)-(+)-2-chloro-2-phenylethyl p-tolyl sulfone 
• 71899-81-5 (R)-(+)-2-hydroxy-2-phenylethyl p-tolyl sulfone 
• 105769-46-8 (R)-(+)-2-chloro-2-phenylethyl phenyl sulfone 
• 167156-83-4 (R)-2-<(4-methoxyphenyl)sulfanyl>-1-phenylethanol 
• 96938-08-8 (R)-(+)-2-hydroxy-2-phenylethyl p-tolyl sulfide 
• 109183-57-5 (R)-(+)-2-chloro-2-phenylethyl methyl sulfone 
• 5324-56-1 (R)-2-(methylsulfonyl)-1-phenylethanol 
• 121053-49-4 (R)-(+)-1-phenyl-2-(phenylthio)ethan-1-ol 
• 120886-82-0 (R)-1-phenyl-2-(phenylsulfonyl)ethanol 
• 111613-52-6 (R)-2-methylthio-1-phenyl-ethanol 
• 60168-63-0 (R)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethanol 
• 133811-88-8 (4R,14R)-(-)-4,14-diphenyl-3,6,9,12,15-pentaoxa-21-azabicyclo<15.3.1>heneicosa-1(21),17,19-triene 
• 121917-51-9 (R,R)-(-)-1,11-diphenyl-3,6,9-trioxaundecane-1,11-diol 

Relevant articles and documents

Asymmetric Radical Reaction in the Coordination Sphere. 2. Asymmetric Addition of Alkane- and Arenesulfonyl Chlorides to Olefins Catalyzed by a Ruthenium(II)-Phosphine Complex with Chiral Ligands

The addition of arenesulfonyl chlorides to styrene in the presence of a catalytic amount of a ruthenium(II) complex with chiral phosphine ligands, Ru2Cl43 or Ru2Cl43, proceeds under mild conditions to give optically active 1:1 adducts,

Enantiomerically Pure Acetals in Organic Synthesis. 1. Chromatographic Separability of Furanoside and Pyranoside Acetals Derived from α-Hydroxy Esters

A general chromatographic separation of diastereomeric furanoside and pyranoside acetals derived from α-hydroxy esters is described.Application of this separation methodology is made to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxy-β-erythro-pentopyranoside.