dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Base Information

Chemical Name:dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside
CAS No.:869216-46-6
Molecular Formula:C₃₁H₄₂O₇
Molecular Weight:526.67
Hs Code.:

Synonyms:dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Suppliers and Price of dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

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 dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

There total 5 articles about dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside 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: 93.0%

: 869216-45-5
C₃₃H₄₄O₈

: 869216-46-6
dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: With methanol; acetyl chloride; at 20 ℃; for 14h;
DOI:10.1055/s-2005-872674

Reference yield:

: 5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranose

: 869216-46-6
dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / K₂CO₃ / CH₂Cl₂ / 12 h / 20 °C

2: 89 percent / TMSOTf / CH₂Cl₂ / 3 h / 20 °C

3: 93 percent / AcCl; MeOH / 14 h / 20 °C

With methanol; trimethylsilyl trifluoromethanesulfonate; potassium carbonate; acetyl chloride; In dichloromethane;
DOI:10.1055/s-2005-872674

Reference yield:

: 869216-43-3
C₂₃H₂₂O₉

: 869216-46-6
dodecyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / BnNH₂ / tetrahydrofuran / 24 h / 20 °C

2: 86 percent / K₂CO₃ / CH₂Cl₂ / 12 h / 20 °C

3: 89 percent / TMSOTf / CH₂Cl₂ / 3 h / 20 °C

4: 93 percent / AcCl; MeOH / 14 h / 20 °C

With methanol; trimethylsilyl trifluoromethanesulfonate; potassium carbonate; acetyl chloride; benzylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1055/s-2005-872674