α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

Base Information

Chemical Name:α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol
CAS No.:123487-64-9
Molecular Formula:C₃₀H₅₃NO₂₅
Molecular Weight:827.743
Hs Code.:

Synonyms:α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

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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 α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

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Technology Process of α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

There total 3 articles about α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol 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: 100.0%

: 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-benzyl-α-D-mannopyranosyl-(1->4)-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1->6)-2,3,4,5-tetra-O-benzyl-D-myo-inositol

: 123487-64-9
α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; water; at 20 ℃; for 12h;
DOI:10.1081/CAR-200066956

Reference yield:

: C₉₄H₁₀₇NO₂₇

: 123487-64-9
α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

Guidance literature:: With formic acid; palladium on activated charcoal; In methanol; for 2h; Yield given;
DOI:10.1021/ja00110a011

Reference yield:

: 123487-62-7,123538-45-4
O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1-2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-pent

: 123487-64-9
α-D-mannopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-α-D-mannopyranosyl-(1->4)-2-amino-2-deoxy-α-D-glucopyranosyl-(1->6)-D-myo-inositol

Guidance literature:: With palladium on activated charcoal; formic acid; sodium methylate; Yield given. Multistep reaction; 1.) MeOH, 2.) MeOH;
DOI:10.1021/ja00204a049