112344-80-6

Basic information

• Product Name: 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside
• Synonyms: 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside
• CAS NO: 112344-80-6
• Molecular Weight: 580.721
• Mol File: 112344-80-6.mol
• Article Data: 38

Chemical Properties

• CAS DataBase Reference: 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside(112344-80-6)
• EPA Substance Registry System: 2-propenyl 2,3,4,6-tetra-O-benzyl-α-D-glactopyranoside(112344-80-6)

Safety Data

• Hazardous Substances Data: 112344-80-6(Hazardous Substances Data)

Upstream product

• 53008-62-1 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl iodide 
• 107-18-6 allyl alcohol 
• 1693-71-6 tris(allyl)borate 
• 3866-62-4 2,3,4,6-tetra-O-benzyl-D-galactopyranosyl acetate 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 63053-84-9 1-O-benzoyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranose 
• 864811-23-4 2,3,4,6-tetra-O-benzyl-1-O-[N-allyl-thiocarbamoyl]-D-galactopyranose 
• 604-69-3 β-D-glucose pentaacetate 
• 194088-16-9 1-O-propargyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 214333-70-7 2-oxopropyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 34272-02-1 1-O-propargyl 2,3,4,6-tetra-O-acetyl-β-D-glucose 
• 34272-03-2 propargyl β-D-glucopyranoside 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 

Downstream Products

• 869711-61-5 (RS)-(2,3-epoxy-1-propyl) 2,3,4,6-tetra-O-benzyl-α-D-galactopyranoside 
• 479637-19-9 (2R,3S,4S,5R,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-[((E)-nonadec-2-enyl)oxy]-tetrahydro-pyran 
• 479637-21-3 (2S,3S)-1-((2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-nonadecane-2,3-diol 
• 479637-20-2 (2R,3R)-1-((2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-nonadecane-2,3-diol 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 59531-24-7 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 88567-49-1 6-O-acetyl-2,3,4-tri-O-benzyl-α/β-D-galactopyranoside 
• 61277-56-3 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α/β-D-galactopyranose 
• 168253-07-4 (2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-ethynyl-tetrahydro-pyran 
• 141196-28-3 trimethyl(((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)ethynyl)silane 
• 168105-48-4 C₇₂H₇₀O₁₀ 
• 1384643-96-2 C₄₅H₄₄N₂O₆ 
• 1384643-91-7 C₄₃H₄₃NO₆ 

Relevant articles and documents

ALLYL ETHYL CARBONATE/PALLADIUM(0), A NEW SYSTEM FOR THE ONE STEP CONVERSION OF ALCOHOLS INTO ALLYL ETHERS UNDER NEUTRAL CONDITIONS

Alcohols are converted in a one-step procedure into allyl ethers under neutral conditions, using allyl ethyl carbonate in the presence of a catalytic amount of palladium(0).Anomeric hydroxyls are selectively allylated in the presence of other hydroxyl gro

N-benzoylglycine/thiourea cooperative catalyzed stereoselective O-glycosidation: Activation of O-glycosyl trichloroacetimidate donors

A new practical utility for β-stereoselective glycosylation via activation of O-glycosyl trichloroacetimidate donors using N-benzoylglycine/thiourea cooperative catalysis has been demonstrated. This method represents the first instance where amino acid derived N-benzoylglycine is used as a catalyst for O–glycosylation under mild reaction conditions at ambient temperature. NMR spectroscopy studies suggest that thiourea cocatalyst exhibit a cooperative behaviour that has a strong effect on the reaction rate, yield, and the β-selectivity.

Tris(pentafluorophenyl)borane-promoted stereoselective glycosylation with glycosyl trichloroacetimidates under mild conditions

Tris(pentafluorophenyl)borane-promoted stereoselective glycosylation with trichloroacetimidate glycosyl donors is described. The reactions proceed efficiently with a wide range of acceptors, from sugar to nonsugar, under mild conditions in the presence of