p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

Base Information

Chemical Name:p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside
CAS No.:1241380-41-5
Molecular Formula:C₂₀H₁₈O₆
Molecular Weight:354.359
Hs Code.:

Synonyms:p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

Suppliers and Price of p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

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Technology Process of p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

There total 1 articles about p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside 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%

: 442894-26-0
p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside

: 1241380-41-5
p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

Guidance literature:: With dipyridinium dichromate; In dichloromethane; at 25 ℃; for 18h; Inert atmosphere;
DOI:10.1039/c004204h

Reference yield:

: 1241380-41-5
p-methoxyphenyl 6-O-benzoyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

: 1241380-42-6
6-O-benzoyl-2,3-dideoxy-D-glycelo-hex-2-enopyranos-4-ulose

: 6-O-benzoyl-2,3-dideoxy-D-glycelo-hex-2-enopyranos-4-ulose

Guidance literature:: With ammonium cerium (IV) nitrate; In water; acetonitrile; at 25 ℃; for 1h; optical yield given as %de;
DOI:10.1039/c004204h