octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Base Information

Chemical Name:octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside
CAS No.:950602-99-0
Molecular Formula:C₆₃H₆₈O₁₅
Molecular Weight:1065.22
Hs Code.:

Synonyms:octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Suppliers and Price of octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

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 octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

There total 5 articles about octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside 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: 89.0%

: 950602-83-2
4-methylphenyl 2,3,4,6-tetra-O-benzoyl-1-thio-α-D-mannopyranoside

: 950602-92-3
octyl 3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

: 950602-99-0
octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Guidance literature:: With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃;
DOI:10.1016/j.carres.2007.05.001

Reference yield:

: 195704-64-4
octyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

: 950602-99-0
octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH / dimethylformamide / 0.17 h / cooling

1.2: 94 percent / dimethylformamide / 1 h / 20 °C

2.1: 66 percent / AlCl₃; LiAlH₄ / diethyl ether; CH₂Cl₂ / 20 °C

3.1: 89 percent / N-iodosuccinimide; TMSOTf / CH₂Cl₂ / 0 °C

With N-iodo-succinimide; lithium aluminium tetrahydride; aluminium trichloride; trimethylsilyl trifluoromethanesulfonate; sodium hydride; In diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2007.05.001

Reference yield:

: 950602-94-5
octyl 2,3:4,6-di-O-benzylidene-α-D-mannopyranoside

: 950602-99-0
octyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-3,4-di-O-benzyl-2-O-methyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: 32 percent / AlCl₃; LiAlH₄ / diethyl ether; CH₂Cl₂ / 0 °C

2.1: NaH / dimethylformamide / 0.17 h / cooling

2.2: 94 percent / dimethylformamide / 1 h / 20 °C

3.1: 66 percent / AlCl₃; LiAlH₄ / diethyl ether; CH₂Cl₂ / 20 °C

4.1: 89 percent / N-iodosuccinimide; TMSOTf / CH₂Cl₂ / 0 °C

With N-iodo-succinimide; lithium aluminium tetrahydride; aluminium trichloride; trimethylsilyl trifluoromethanesulfonate; sodium hydride; In diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.carres.2007.05.001