(2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Base Information

Chemical Name:(2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol
CAS No.:351070-52-5
Molecular Formula:C₂₆H₃₄O₈
Molecular Weight:474.551
Hs Code.:

Synonyms:(2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Suppliers and Price of (2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of (2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

There total 2 articles about (2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol 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: 95.0%

: 221462-07-3
(2'R,3'R)-1D-3-O-[(S)-(+)-O-acetylmandelyl]-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

: 351070-52-5
(2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Guidance literature:: With sodium hydroxide; In methanol; for 1h; Heating;
DOI:10.1021/jm0005499

Reference yield:

: (2'RS,3'RS)-DL-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

: 351070-52-5
(2'R,3'R)-1D-1,4-di-O-benzyl-5,6-O-(2',3'-dimethoxybutane-2',3'-diyl)-myo-inositol

Guidance literature:: Multi-step reaction with 2 steps

1: 34 percent / DCC; DMAP / CH₂Cl₂ / 1 h / -20 °C

2: 95 percent / NaOH / methanol / 1 h / Heating

With dmap; sodium hydroxide; dicyclohexyl-carbodiimide; In methanol; dichloromethane;
DOI:10.1021/jm0005499