11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

Base Information

Chemical Name:11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside
CAS No.:1140530-91-1
Molecular Formula:C₅₁H₅₈O₁₁
Molecular Weight:847.015
Hs Code.:

Synonyms:11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

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Technology Process of 11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

There total 1 articles about 11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-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: 81.0%

: 166828-15-5
4,5,6,8-tetra-O-benzyl-1,2-dideoxy-α-D-gluco-oct-1-eno-3-ulopyranose

: 127017-97-4
2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl benzoate

: 1140530-91-1
11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

Guidance literature:: With bismuth(lll) trifluoromethanesulfonate; calcium sulfate; In dichloromethane; at 0 ℃; for 24h;
DOI:10.3390/molecules13081840

Reference yield:

: 1140530-91-1
11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside

: C₅₀H₅₆O₁₂

Guidance literature:: 11-benzyloxy-3,6,9-trioxaundecyl 2,3,4,6-tetra-O-benzyl-1-C-vinyl-α-D-glucopyranoside; With ozone; In dichloromethane; at -78 ℃; for 5h;

With triphenylphosphine; In dichloromethane; at 20 ℃; for 19h; Further stages.;
DOI:10.3390/molecules13081840