8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Base Information

Chemical Name:8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
CAS No.:1323024-78-7
Molecular Formula:C₂₈H₃₈BrCl₃N₄O₁₃
Molecular Weight:824.892
Hs Code.:

Synonyms:8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Suppliers and Price of 8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-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-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

There total 5 articles about 8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-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:

: 2186-92-7
p-Anisaldehyde dimethyl acetal

: C₂₀H₃₂BrCl₃N₄O₁₂

: 1323024-78-7
8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Guidance literature:: With 10-camphorsufonic acid; In acetonitrile; for 2h;
DOI:10.1016/j.carres.2011.02.011

Reference yield:

: 1323024-76-5
8-azido-3,6-dioxaoctyl 4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside

: 1323024-78-7
8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide; barium carbonate / tetrachloromethane; 1,1,2,2-tetrachloroethane / 2 h / 100 °C

2.1: sodium methylate / methanol

2.2: amberlite IR-120

3.1: 10-camphorsufonic acid / acetonitrile / 2 h

With N-Bromosuccinimide; 10-camphorsufonic acid; sodium methylate; barium carbonate; In methanol; tetrachloromethane; acetonitrile; 1,1,2,2-tetrachloroethane;
DOI:10.1016/j.carres.2011.02.011

Reference yield:

: 399035-92-8
ethyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-4,6-O-benzylidene-2-deoxy-1-thio-2-trichloroacetamido-β-D-glucopyranoside

: 1323024-78-7
8-azido-3,6-dioxaoctyl 6-bromo-2,6-dideoxy-2-trichloroacetamido-3-O-(4,6-O-p-methoxybenzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-iodo-succinimide; silver trifluoromethanesulfonate / dichloromethane / 1 h / -10 °C / Inert atmosphere; Molecular sieve

2.1: N-Bromosuccinimide; barium carbonate / tetrachloromethane; 1,1,2,2-tetrachloroethane / 2 h / 100 °C

3.1: sodium methylate / methanol

3.2: amberlite IR-120

4.1: 10-camphorsufonic acid / acetonitrile / 2 h

With N-Bromosuccinimide; N-iodo-succinimide; 10-camphorsufonic acid; sodium methylate; silver trifluoromethanesulfonate; barium carbonate; In methanol; tetrachloromethane; dichloromethane; acetonitrile; 1,1,2,2-tetrachloroethane;
DOI:10.1016/j.carres.2011.02.011