8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

Base Information

Chemical Name:8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside
CAS No.:84439-24-7
Molecular Formula:C₃₃H₄₅NO₉
Molecular Weight:599.722
Hs Code.:

Synonyms:8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

Suppliers and Price of 8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

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 8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

There total 1 articles about 8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside 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: 79.0%

: 3587-60-8
Benzyloxymethyl chloride

: 71048-95-8
ω-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 84439-24-7
8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

Guidance literature:: With 2,6-dimethylpyridine; In acetonitrile; at 80 ℃; for 12h;
DOI:10.1016/0008-6215(82)84034-2

Reference yield: 12.0%

: 84439-24-7
8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

: 84439-25-8
8-methoxycarbonyloctyl 2-acetamido-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

: 65567-18-2
8-methoxycarbonyloctyl 2-acetamido-2-deoxy-β-D-glucopyranoside

Guidance literature:: With acetic acid; In 1,4-dioxane; at 80 ℃; for 1.25h;
DOI:10.1016/0008-6215(82)84034-2

Reference yield:

: 84439-24-7
8-methoxycarbonyloctyl 2-acetamido-4,6-O-benzylidene-3-O-benzyloxymethyl-2-deoxy-β-D-glucopyranoside

: 84455-81-2
8-methoxycarbonyloctyl 2-acetamido-3,6-di-O-benzyloxymethyl-2-deoxy-4-O-(3,4,6-tri-O-benzyl-2-O-p-nitrobenzoyl-α-D-galactopyranosyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / 50percent aq. AcOH / dioxane / 1.25 h / 80 °C

2: 2,6-lutidine / dimethylformamide / 16 h / Ambient temperature

3: CF₃SO₂OAg / CH₂Cl₂; various solvent(s) / 42 h / Ambient temperature

With 2,6-dimethylpyridine; silver trifluoromethanesulfonate; acetic acid; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(82)84034-2