2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

Base Information

Chemical Name:2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate
CAS No.:1035456-77-9
Molecular Formula:C₅₅H₅₅N₃O₁₁
Molecular Weight:934.055
Hs Code.:

Synonyms:2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

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Chemical Property of 2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

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Technology Process of 2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

There total 1 articles about 2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate 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: 20.0%

: 220712-46-9
3,4,5-tri-O-benzyl-1D-myo-inositol

: 220688-25-5
O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α/β-D-glucopyranosyl) trichloroacetimidate

: 1035456-76-8
N-(2-azido-3,4,6-tri-O-benzyl-1,2-dideoxy-α-D-glucopyranosyl)trichloroacetamide

: 1035456-77-9
2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

: 1035456-73-5
2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyI-(1-6)-3,4,5-tri-O-benzyl-D-myo-inositol-1,2-cyclic carbonate

Guidance literature:: 3,4,5-tri-O-benzyl-1D-myo-inositol; O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α/β-D-glucopyranosyl) trichloroacetimidate; With molecular sieve; trifluorormethanesulfonic acid; In diethyl ether; at -20 - 20 ℃;

With sodium hydrogencarbonate; In diethyl ether; for 0.25h;