dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Base Information

Chemical Name:dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate
CAS No.:1562507-80-5
Molecular Formula:C₆₄H₇₁O₁₃P
Molecular Weight:1079.23
Hs Code.:

Synonyms:dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Suppliers and Price of dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

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 dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

There total 3 articles about dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate 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: 86.0%

: 1562507-78-1
2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl methyl iodide

: 121-45-9
phosphorous acid trimethyl ester

: 1562507-80-5
dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Guidance literature:: at 20 ℃; for 24h; Reflux;
DOI:10.1016/j.bmc.2013.12.058

Reference yield:

: 1562507-65-6
3,4,7-tri-O-benyl-5-O-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)-D-glucphept-1-enitol

: 1562507-80-5
dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 3 h / 20 °C

2: potassium chloride / tetrahydrofuran; water / 20 °C

3: iodine / dichloromethane / 1 h / 20 °C

4: 24 h / 20 °C / Reflux

With potassium chloride; iodine; In tetrahydrofuran; dichloromethane; water; 4: |Michaelis-Arbuzov Synthesis;
DOI:10.1016/j.bmc.2013.12.058

Reference yield:

: 2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl methyl mercuric chloride

: 1562507-80-5
dimethyl (2,3,6,2',3',4',6'-hepta-O-benzyl-α-D-maltosyl)methylphosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: iodine / dichloromethane / 1 h / 20 °C

2: 24 h / 20 °C / Reflux

With iodine; In dichloromethane; 2: |Michaelis-Arbuzov Synthesis;
DOI:10.1016/j.bmc.2013.12.058