126330-72-1

Basic information

• Product Name: (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran
• Synonyms: (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran
• CAS NO: 126330-72-1
• Molecular Weight: 634.767
• Mol File: 126330-72-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran(126330-72-1)
• EPA Substance Registry System: (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran(126330-72-1)

Safety Data

• Hazardous Substances Data: 126330-72-1(Hazardous Substances Data)

Upstream product

• 59055-61-7 2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl bromide 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 136984-94-6 2-pyridyl 2,3,4-tri-O-acetyl-1-thio-α/β-L-rhamnoyranoside 
• 100-39-0 benzyl bromide 
• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 
• 126330-69-6 2-pyridyl 2,3,4-tri-O-benzyl-1-thio-α,β-L-rhamnopyranoside 
• 33639-77-9 perbenzyl fucosyl bromide 
• 116514-50-2 ethyl 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside 

Relevant articles and documents

A Mechanistic Probe into 1,2-cis Glycoside Formation Catalyzed by Phenanthroline and Further Expansion of Scope

Phenanthroline, a rigid and planar compound with two fused pyridine rings, has been used as a powerful ligand for metals and a binding agent for DNA/RNA. We discovered that phenanthroline could be used as a nucleophilic catalyst to efficiently access high

Stereoselective synthesis of α-linked saccharides by use of per O-benzylated 2-pyridyl 1-thio hexopyranosides as glycosyl donors and methyl iodide as an activator

A new, practical, stereoselective glycosidation methodology is described where per O-benzylated 2-pyridyl 1-thio-α/β-hexopyranosyl donors of D-gluco-(1), D-galacto- (2), D-manno- (3) and L-rhamno- (4) configurations have been efficiently coupled with dive

A MILD GENERAL METHOD FOR THE SYNTHESIS OF α-LINKED DISACCHARIDES

Stereoselective α-glycosylations may be achieved using stable 2-pyridyl thioglycosides (anomeric mixture) having a non-participating 2-substituent as glycosyl donor and methyl iodide as an activator.