O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

Base Information

Chemical Name:O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine
CAS No.:128377-12-8
Molecular Formula:C₉₆H₁₅₁NO₂₈Si
Molecular Weight:1795.33
Hs Code.:

O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

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Suppliers and Price of O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

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Chemical Property of O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

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Technology Process of O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

There total 1 articles about O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine 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:

: 557-59-5
n-tetracosanoic acid

: C₇₂H₁₀₅NO₂₇Si

: 128377-12-8
O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

Guidance literature:: With tributyl-amine; 2-chloro-1-methyl-pyridinium iodide; In dichloromethane; at 20 ℃; for 3h; Yield given;
DOI:10.1016/0008-6215(90)84167-S

Reference yield:

: 128377-12-8
O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-mannopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->1)-3-O-tert-butyldiphenylsilyl-2N-tetracosanoyl-(4E)-sphingenine

: 113421-38-8,128443-10-7
O-α-D-mannopyranosyl-(1->3)-O-β-D-mannopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->1)-2-N-tetracosanoyl-(4E)-sphingenine

Guidance literature:: With tetrabutyl ammonium fluoride; sodium methylate; Yield given. Multistep reaction; 1) oxolane, 1h, 20 deg C, 2) oxolane, MeOH, 20h, 20 deg C;
DOI:10.1016/0008-6215(90)84167-S