Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

Base Information

Chemical Name:Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside
CAS No.:126990-50-9
Molecular Formula:C₈₁H₈₆O₂₅
Molecular Weight:1459.56
Hs Code.:

Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

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Suppliers and Price of Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

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Chemical Property of Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

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Technology Process of Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

There total 1 articles about Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside 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:

: 126990-54-3
Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-α-D-glucopyranoside

: 5158-64-5
2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide

: 126990-50-9
Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

Guidance literature:: With molecular sieve; mercury dibromide; mercury(II) oxide; Yield given. Multistep reaction; CH₂Cl₂, 1) room temp., 1 h; 2) 2 h, room temp.;
DOI:10.1016/0008-6215(90)84272-V

Reference yield:

: 126990-50-9
Allyl O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-(1->2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->2)-O-<2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->6)>-3-O-benzyl-α-D-glucopyranoside

: 126990-49-6
Propyl O-α-D-arabinofuranosyl-(1->2)-O-α-D-mannopyranosyl-(1->2)-O-α-L-rhamnopyranosyl-(1->6)-α-D-glucopyranoside

Guidance literature:: With hydrogen; sodium methylate; palladium on activated charcoal; Yield given. Multistep reaction; 1) pH 8, methanol, room temp.; 2) 18 h, 1 atm;
DOI:10.1016/0008-6215(90)84272-V