1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Base Information

Chemical Name:1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose
CAS No.:125568-59-4
Molecular Formula:C₅₁H₆₄O₁₁Si
Molecular Weight:881.148
Hs Code.:

Synonyms:1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Suppliers and Price of 1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

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 1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

There total 3 articles about 1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose 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:

: 79834-15-4
(2-bromo-3,5-bis(methoxymethoxy)phenyl)methanol

: 125568-59-4
1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / imidazole / dimethylformamide / 5 h

2: 1.) butyllithium / 1.) ether, -80 deg C, 30 min, 2a.) -80 deg C, 1 h, 2.) from -80 deg C to 15 deg C, 3 h

With 1H-imidazole; n-butyllithium; In N,N-dimethyl-formamide;

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 125568-59-4
1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / imidazole / dimethylformamide / 5 h

2: 1.) butyllithium / 1.) ether, -80 deg C, 30 min, 2a.) -80 deg C, 1 h, 2.) from -80 deg C to 15 deg C, 3 h

With 1H-imidazole; n-butyllithium; In N,N-dimethyl-formamide;

Reference yield:

: 13096-62-3
(3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one

: 125568-62-9
2-bromo-1-<(tertbutyldimethylsilyl)oxy>-3,5-bis(methoxymethoxy)benzene

: 125568-59-4
1-C-<6-<<(tert-butyldimethylsilyl)oxy>methyl>-2,4-bis(methoxymethoxy)phenyl>-2,3,4,6-tetra-O-benzyl-D-glucose

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) ether, -80 deg C, 30 min, 2a.) -80 deg C, 1 h, 2.) from -80 deg C to 15 deg C, 3 h;