103616-05-3

Basic information

• Product Name: (2S,3S,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>-2-pentanol
• Synonyms: (2S,3S,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>-2-pentanol
• CAS NO: 103616-05-3
• Molecular Weight: 314.379
• Mol File: 103616-05-3.mol

Chemical Properties

• CAS DataBase Reference: (2S,3S,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>-2-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>-2-pentanol(103616-05-3)
• EPA Substance Registry System: (2S,3S,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>-2-pentanol(103616-05-3)

Safety Data

• Hazardous Substances Data: 103616-05-3(Hazardous Substances Data)

Upstream product

• 74-83-9 methyl bromide 
• 99878-63-4 4-O-benzyl-2,3-O-bis(methoxymethyl)-L-threose 
• 1256248-86-8 C₂₃H₃₂O₉S 
• 103499-50-9 (3R,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>pentan-2-one 

Downstream Products

• 103499-50-9 (3R,4S)-5-(benzyloxy)-3,4-bis<(methoxymethyl)oxy>pentan-2-one 
• 1256248-87-9 1-(((2S,3S,4S)-2,3,4-tris(methoxymethoxy)pentyloxy)methyl)benzene 

Relevant articles and documents

Stereoselective total synthesis of (+)-anamarine via cross-metathesis protocol

A convergent stereoselective total synthesis of (+)-anamarine via cross-metathesis (CM) protocol starting from 2-butyn-1,4-diol and vinyl lactone is reported. Other key features of the strategy include the use of Sharpless asymmetric epoxidation, Sharples

α-Chelation Controlled Nucleophilic Addition to Chiral α,β-Dialkoxy Carbonyl Compounds. Diastereoselective Preparation of L-xylo and L-lyxo Triols

The Grignard reaction of 4-O-benzyl-2,3-O-bis(methoxymethyl)-L-threose (1) or 2,3-O-bis(methoxymethyl)-L-threo-furanose (4) with RMgX (R = Me, n-Pr, p-MeOC6H4, and p-MeOC6H4CH2) provided the chromatographically separable mixtures of the xylo and lyxo alco