79723-92-5

Basic information

• Product Name: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose
• Synonyms: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose
• CAS NO: 79723-92-5
• Molecular Weight: 759.764
• Mol File: 79723-92-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose(79723-92-5)
• EPA Substance Registry System: 1,6-Anhydro-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose(79723-92-5)

Safety Data

• Hazardous Substances Data: 79723-92-5(Hazardous Substances Data)

Upstream product

• 55287-63-3 1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 100-39-0 benzyl bromide 
• 70831-94-6 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranosyl bromide 
• 61074-17-7 1,6-Anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 

Downstream Products

• 3645-45-2 phthaloyldihydrazine 
• 79705-52-5 3-O-(2-Acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-1,6-anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 79705-55-8 1,6-Di-O-acetyl-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranose 
• 79705-54-7 1,6-Di-O-acetyl-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-galactopyranose 
• 79705-56-9 3-O-(2-Acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-1,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranose 

Relevant articles and documents

Bausteine von Oligosacchariden, XXIX. Synthese des Trisaccharids aus N-Acetylglucosamin, Galactose und Rhamnose einer O-determinanten Kette von Escherichia coli. Abhaengigkeit der Stereoselektivitaet der α-Glycosidsynthese von der Reaktivitaet des Pyranos

The mercury salt catalysed reaction of substituted α-D-galactosyl halides with the reactive 4-OH groups of the rhamnosides 18 and 19 were studied.The order of reactivity of the halides increases with the following substituents: O-acetyl O-glucosyl O-b