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allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside

Base Information
  • Chemical Name:allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside
  • CAS No.:1343987-75-6
  • Molecular Formula:C50H56O11
  • Molecular Weight:832.988
  • Hs Code.:
allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside

Synonyms:allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside

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Chemical Property of allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside
Chemical Property:
Purity/Quality:
Safty Information:
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Technology Process of allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside

There total 13 articles about allyl 2-O-benzyl-3-O(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glycopyranoside 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:
Guidance literature:
With acetic acid; In water; at 50 ℃; for 4h; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 8 steps
1.1: sodium methylate / methanol / 3 h / 20 °C
1.2: 0.5 h / 0 °C
1.3: 20 °C
2.1: sodium hydrogencarbonate; Oxone / dichloromethane; water; acetone / 2 h
2.2: 20 °C
3.1: dmap / dichloromethane / 18 h / 20 °C
4.1: hydrogen / (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate / tetrahydrofuran / Inert atmosphere
4.2: 2 h
5.1: potassium carbonate / dichloromethane / 8 h / 20 °C
6.1: dichloromethane / 0.17 h / AW-300 molecular sieves
6.2: 0.5 h / 0 °C
7.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C
7.2: 18 h / 20 °C
8.1: acetic acid / water / 4 h / 50 °C
With dmap; Oxone; hydrogen; sodium methylate; sodium hydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; mineral oil;
Guidance literature:
Multi-step reaction with 8 steps
1.1: sodium methylate / methanol / 3 h / 20 °C
1.2: 0.5 h / 0 °C
1.3: 20 °C
2.1: sodium hydrogencarbonate; Oxone / dichloromethane; water; acetone / 2 h
2.2: 20 °C
3.1: dmap / dichloromethane / 18 h / 20 °C
4.1: hydrogen / (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate / tetrahydrofuran / Inert atmosphere
4.2: 2 h
5.1: potassium carbonate / dichloromethane / 8 h / 20 °C
6.1: dichloromethane / 0.17 h / AW-300 molecular sieves
6.2: 0.5 h / 0 °C
7.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C
7.2: 18 h / 20 °C
8.1: acetic acid / water / 4 h / 50 °C
With dmap; Oxone; hydrogen; sodium methylate; sodium hydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; mineral oil;
upstream raw materials:

benzyl bromide

D-Glucose

3,4,6-tri-O-benzyl-D-glucal

D-glucal triacetate

Downstream raw materials:

C114H128O23

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