D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Base Information

Chemical Name:D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol
CAS No.:157542-48-8
Molecular Formula:C₆₈H₇₂O₁₈P₄
Molecular Weight:1301.2
Hs Code.:

Synonyms:D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Suppliers and Price of D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

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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 D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Chemical Property:

Purity/Quality:

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Technology Process of D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

There total 4 articles about D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-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:

: C₆₈H₇₂O₁₄P₄

: 157542-48-8
D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Guidance literature:: With peracetic acid; In acetonitrile; Yield given;

Reference yield:

: 57029-87-5,1251832-23-1
(±)-1,2-cyclohexylidene myo-inositol

: 157542-48-8
D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-tetrazole / acetonitrile / 2 h / Ambient temperature

2: 30percent CH₃CO₃H / acetonitrile

With 1H-tetrazole; peracetic acid; In acetonitrile;

Reference yield:

: 108549-23-1
Dibenzyl N,N-diisopropylphosphoramidite

: 157542-48-8
D-2,3-O-cyclohexylidene-1,4,5,6-tetra-O-(bisbenzyloxyphosphoryl)-myo-inositol

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-tetrazole / acetonitrile / 2 h / Ambient temperature

2: 30percent CH₃CO₃H / acetonitrile

With 1H-tetrazole; peracetic acid; In acetonitrile;