124718-61-2

Basic information

• Product Name: (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran
• Synonyms: (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran
• CAS NO: 124718-61-2
• Molecular Weight: 556.723
• Mol File: 124718-61-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(124718-61-2)
• EPA Substance Registry System: (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-6-methoxy-5-phenylsulfanyl-tetrahydro-pyran(124718-61-2)

Safety Data

• Hazardous Substances Data: 124718-61-2(Hazardous Substances Data)

Upstream product

• 1262390-58-8 C₂₀H₂₄O₅S 
• 100-39-0 benzyl bromide 
• 67-56-1 methanol 
• 55628-54-1 (2R,3S,4S)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-3,4-dihydro-2H-pyran 

Relevant articles and documents

A tandem Michael-SN2-mediated general route to six-membered heterocycles and carbocycles

A powerful, flexible, and stereoselective general strategy for the construction of chirally pure six-membered heterocycles and carbocycles by utilizing a tandem Michael-SN2 sequence is described. The strategy avoids the tedious synthesis of sep

Aureolic acid antibiotics: A simple method for 2-deoxy-β-glycosidation

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