(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Base Information

Chemical Name:(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose
CAS No.:1333231-18-7
Molecular Formula:C₄₂H₄₃N₃O₁₆
Molecular Weight:845.814
Hs Code.:

Synonyms:(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Suppliers and Price of (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

There total 8 articles about (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose 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: 70.0%

: 1333231-16-5
2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl trichloroacetimidate

: 578007-57-5
allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

: 1333231-18-7
(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -30 - 20 ℃; Inert atmosphere;
DOI:10.1039/c1cc13213j

Reference yield:

: 1333231-07-4
3,4-di-O-acetyl-6-O-tosyl-1,2-O-ethylidene-β-D-mannopyranoside

: 1333231-18-7
(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium azide / N,N-dimethyl-formamide / Inert atmosphere

2.1: trifluoroacetic acid / water / Inert atmosphere

2.2: Inert atmosphere

3.1: acetic acid; hydrazine / Inert atmosphere

3.2: Inert atmosphere

4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 20 °C / Inert atmosphere

5.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / -30 - 20 °C / Inert atmosphere

With sodium azide; trimethylsilyl trifluoromethanesulfonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; trifluoroacetic acid; hydrazine; In dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1039/c1cc13213j

Reference yield:

: 1333231-08-5
3,4-di-O-acetyl-6-azido-1,2-O-ethylidene-β-D-mannopyranoside

: 1333231-18-7
(2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid / water / Inert atmosphere

1.2: Inert atmosphere

2.1: acetic acid; hydrazine / Inert atmosphere

2.2: Inert atmosphere

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 20 °C / Inert atmosphere

4.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / -30 - 20 °C / Inert atmosphere

With trimethylsilyl trifluoromethanesulfonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; trifluoroacetic acid; hydrazine; In dichloromethane; water;
DOI:10.1039/c1cc13213j