allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

Base Information

Chemical Name:allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside
CAS No.:666845-76-7
Molecular Formula:C₅₀H₄₆O₁₄
Molecular Weight:870.907
Hs Code.:

Synonyms:allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

Suppliers and Price of allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

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 allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

There total 1 articles about allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside 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: 84.0%

: 161007-95-0
2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyltrichloroacetimidate

: 518975-31-0
allyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside

: 666845-76-7
allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -20 - 20 ℃; for 3h;
DOI:10.1016/j.carres.2003.09.014

Reference yield: 78.0%

: 666845-76-7
allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

: 666845-77-8
C₄₇H₄₂O₁₄

Guidance literature:: palladium dichloride; In methanol; at 20 ℃; for 2h;
DOI:10.1016/j.carres.2003.09.014

Reference yield:

: 666845-76-7
allyl 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1-> 2)-3,4-di-O-benzoyl-α-L-rhamnoparanoside

: 666845-82-5
C₆₇H₆₀O₂₀

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / PdCl₂ / methanol / 2 h / 20 °C

2: 86 percent / DBU / CH₂Cl₂ / 3 h / 20 °C

3: 79 percent / TMSOTf / CH₂Cl₂ / 3 h / -20 - 20 °C

4: 83 percent / PdCl₂ / methanol / 2 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium dichloride; In methanol; dichloromethane;
DOI:10.1016/j.carres.2003.09.014