89067-99-2

Basic information

• Product Name: benzyl 2,4-di-O-benzyl-β-D-mannopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• Synonyms: benzyl 2,4-di-O-benzyl-β-D-mannopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• CAS NO: 89067-99-2
• Molecular Weight: 1393.55
• Mol File: 89067-99-2.mol

Chemical Properties

• CAS DataBase Reference: benzyl 2,4-di-O-benzyl-β-D-mannopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,4-di-O-benzyl-β-D-mannopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(89067-99-2)
• EPA Substance Registry System: benzyl 2,4-di-O-benzyl-β-D-mannopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1<*>4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(89067-99-2)

Safety Data

• Hazardous Substances Data: 89067-99-2(Hazardous Substances Data)

Upstream product

• 89067-97-0 benzyl O-(3,6-di-O-allyl-2,4-di-O-benzyl-β-D-mannopyranosyl)-(1->4)-O-(3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 

Downstream Products

• 89068-00-8 benzyl O-(2,4-di-O-benzyl-β-D-mannopyranosyl)-(1->4)-O-(2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->)4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Building biologics by chemical synthesis: Practical preparation of Di- and triantennary N-linked glycoconjugates

A unified strategy for the syntheses of bi- and triantennary fully sialylated N-glycans is described. The synthesis capitalizes on a global glycosylation strategy that delivers the desired undeca- and tetradecasaccharide in excellent yields. Finally, conjugation of the glycan to PSMA oligopeptide is described.

Rationally designed syntheses of high-mannose and complex type undecasaccharides

Synthetic routes are described to a high-mannose type triantenary undecasaccharide 1 and a completely protected form 39 of the complex type biantenary undecasaccharide 2 carrying α-(2 → 3)-linked sialic acid residues. Starting from a previously reported t

Synthesis of an octasaccharide fragment of high-mannose-type glycans of glycoproteins

O-(α-D-Mannopyranosyl)-(1->2)-O-(α-D-mannopyranosyl)-(1->3)-O-2)-O-(α-D-mannopyranosyl)-(1->6)>-O-(α-D-mannopyranosyl)-(1->6)-O-(β-D-mannopyranosyl)-(1->4)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->4)-2-acetamido-2-deoxy-glu