2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Base Information

Chemical Name:2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide
CAS No.:403480-82-0
Molecular Formula:C₆₁H₄₉BrO₁₇
Molecular Weight:1133.95
Hs Code.:

Synonyms:2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Suppliers and Price of 2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

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 2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

There total 3 articles about 2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide 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: 90.0%

: 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-D-glucopyranoside

: 403480-82-0
2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1177/1747519820927966

Reference yield: 76.0%

: 536-11-8,645-03-4,902-54-5,3031-35-4,4604-26-6,5340-95-4,5995-99-3,5996-00-9,13299-20-2,13299-21-3,15548-40-0,16750-26-8,16967-97-8,23339-29-9,24822-33-1,33428-65-8,34674-94-7,35867-21-1,37169-69-0,37169-72-5,38533-27-6,50271-70-0,65207-30-9,82729-73-5,95463-59-5,100427-99-4,100430-37-3,100483-14-5,102572-70-3,110658-40-7,123809-47-2,140461-60-5,143615-15-0
gentibiose

: 98-88-4
benzoyl chloride

: 403480-82-0
2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Guidance literature:: gentibiose; benzoyl chloride; With pyridine; In chloroform; for 24h;

With hydrogen bromide; In dichloromethane; acetic acid; for 3h;
DOI:10.1271/bbb.65.2719

Reference yield:

: 544686-94-4
1,2,3,4-tetra-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-α/β-D-glucopyranose

: 403480-82-0
2,3,4,6-tetra-O-benzoyl-β-d-glucopyranosyl-(1→6)-2,3,4-tri-O-benzoyl-α-d-glucopyranosyl bromide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazinium monoacetate / N,N-dimethyl-formamide / 20 °C

2: triphenylphosphine; carbon tetrabromide / dichloromethane / 3 h / 20 °C

With carbon tetrabromide; hydrazinium monoacetate; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1177/1747519820927966