172364-85-1

Basic information

• Product Name: methyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside
• Synonyms: methyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside
• CAS NO: 172364-85-1
• Molecular Weight: 836.801
• Mol File: 172364-85-1.mol

Chemical Properties

• CAS DataBase Reference: methyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside(172364-85-1)
• EPA Substance Registry System: methyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside(172364-85-1)

Safety Data

• Hazardous Substances Data: 172364-85-1(Hazardous Substances Data)

Upstream product

• 34234-44-1 methyl 2,3,4-tri-O-benzoyl-α-D-mannopyranoside 
• 572-10-1 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl chloride 
• 98-88-4 benzoyl chloride 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 259669-42-6 Acetic acid (2R,3aS,5R,6R,7S,7aS)-6-acetoxy-5-acetoxymethyl-2-methyl-2-((2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-[1,3]dioxolo[4,5-b]pyran-7-yl ester 
• 13242-53-0 acetobromomannose 
• 2873-29-2 D-glucal triacetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 311805-99-9 methyl α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-α-D-mannopyranoside 

Relevant articles and documents

"One-pot" access to α-d-mannopyranosides from glycals employing ruthenium catalysis

Ru-catalyzed synthesis of α-d-mannopyranosides from glucal is described via one-pot glycosylation-dihydroxylation reaction. This method is amenable to a variety of acceptors, including carbohydrate-derived and amino-acid containing alcohols to obtain mannosylated peptides and disaccharides.

Regio- and stereoselective synthesis of 1→6 linked manno-, gluco-, and galactopyranose Di-, Tri-, and tetrasaccharides via orthoester intermediates

1→6 linked manno-, gluco-, and galactopyranose di-, tri-, and tetrasaccharides with 1,2-trans glycosidic linkages were concisely and effectively synthesized using peracetylated glycosyl bromides as the donors and unprotected or partially protected glycopy

Synthesis of mono- and dimannoside phosphoramidite derivatives for solid-phase conjugation to oligonucleotides

Mannose and dimannose derivatives have been prepared with an anomerically-linked hydrophobic spacer, and converted to phoshoramidite derivatives suitable for conjugation to oligoribodeoxynucleotides on a DNA/RNA synthesizer. Synthesis of a monomannoside-linked 15-mer oligoribodeoxynucleotide is reported.