(8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

Base Information

Chemical Name:(8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid
CAS No.:79705-71-8
Molecular Formula:C₇₇H₁₀₁NO₂₇
Molecular Weight:1472.64
Hs Code.:

(8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

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Suppliers and Price of (8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

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Chemical Property of (8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

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Technology Process of (8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

There total 1 articles about (8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid 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:

: 79723-95-8
(8-Methoxycarbonyloctyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid

: 79705-68-3
3-O-(2-Acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosylbromid

: (8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-β-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

: 79705-71-8,79733-91-8
(8-Methoxycarbonyloctyl)-4-O-<3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-6-O-acetyl-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-O-benzyl-α-D-galactopyranosyl>-2,3-O-isopropyliden-α-L-rhamnopyranosid

Guidance literature:: With 4 A molecular sieve; mercury(II) cyanide; mercury dibromide; Yield given. Multistep reaction. Yields of byproduct given; 1) CH₂Cl₂, r.t., 2) 0 deg C, CH₂Cl₂;