218607-58-0

Basic information

• Product Name: C₇₀H₇₆O₁₅
• Synonyms: C₇₀H₇₆O₁₅
• CAS NO: 218607-58-0
• Molecular Weight: 1157.36
• Mol File: 218607-58-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₇₀H₇₆O₁₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₇₀H₇₆O₁₅(218607-58-0)
• EPA Substance Registry System: C₇₀H₇₆O₁₅(218607-58-0)

Safety Data

• Hazardous Substances Data: 218607-58-0(Hazardous Substances Data)

Upstream product

• 218607-53-5 (2R,4aR,6R,7R,8S,8aR)-6-((2R,3R,4R,5S,6S)-2-Allyloxy-4,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-3-yloxy)-7,8-bis-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 218607-54-6 (2R,3R,4S,5R,6R)-6-((2R,3R,4R,5S,6S)-2-Allyloxy-4,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-3-yloxy)-4,5-bis-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-ol 
• 219586-38-6 phenylsulfenyl 3-(2',3'-di-O-benzyl-4',6'-O-benzylidene)-β-D-glucopyranoside 
• 158198-56-2 phenyl 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 87470-70-0 S-phenyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-deoxy-1-thio-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 71676-30-7 (2R,4aR,6S,7R,8R,8aS)-2-Phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 128848-51-1 phenyl 3-O-benzyl-4,6-O-benzylidene-1-deoxy-1-thio-β-D-glucopyranoside 
• 218607-57-9 C₇₂H₇₈O₁₆ 

Downstream Products

• 218607-59-1 C₇₃H₇₈N₂O₁₇S 

Relevant articles and documents

Capsular polysaccharide of Streptococcus pneumoniae type 19F: Synthesis of the repeating unit

A new and more versatile synthesis of β-d-ManpNAc-(1→4)-α-d-Glcp-(1→2)-α-l-Rhap, the trisaccharide repeating unit of the Streptococcus pneumoniae type 19F capsular polysaccharide, is described. The present approach allows a simple access to different fragments containing the trisaccharide and the conjugation of the product(s) to a protein through the selective manipulation of the anomeric position at the reducing end and of the HO-4 function at the nonreducing end. The synthetic scheme shows an efficient application of the sulfoxide method for the stereoselective and high yielding formation of the glycosidic linkages. Copyright (C) 1998 Elsevier Science Ltd. A new and more versatile synthesis of β-D-ManpNAc-(1→4)-α-D-Glcp-(1→2)-α-L-Rhap, the trisaccharide repeating unit of the Streptococcus pneumoniae type 19F capsular polysaccharide, is described. The present approach allows a simple access to different fragments containing the trisaccharide and the conjugation of the product(s) to a protein through the selective manipulation of the anomeric position at the reducing end and of the HO-4 function at the nonreducing end. The synthetic scheme shows an efficient application of the sulfoxide method for the stereoselective and high yielding formation of the glycosidic linkages.