2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol

Base Information

• Chemical Name: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol
• CAS No.: 1191118-60-1
• Molecular Formula: C₁₁₂H₁₃₀O₁₈
• Molecular Weight: 1764.25

Synonyms:2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol

Chemical Property of 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol

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Technology Process of 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol

There total 1 articles about 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol (1191118-58-7) + n-hexadecanoyl chloride (112-67-4) → 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol (1191118-60-1)

Guidance literature:

With pyridine; at 20 ℃; for 18h; Inert atmosphere;

DOI:10.1016/j.tetlet.2009.07.109

Reference yield: 81.0%

2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol (1191118-60-1) → (2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol (737788-49-7)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;

DOI:10.1016/j.tetlet.2009.07.109

upstream raw materials:

2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->6)-1-O-(4-methoxybenzyl)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol

n-hexadecanoyl chloride

Downstream raw materials:

(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-palmitoyl-α-D-mannopyranosyl)-D-myo-inositol

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