1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Base Information

Chemical Name:1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol
CAS No.:166184-27-6
Molecular Formula:C₂₄H₃₂O₈
Molecular Weight:448.513
Hs Code.:

Synonyms:1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Suppliers and Price of 1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-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 1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Chemical Property:

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Technology Process of 1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

There total 4 articles about 1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-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: 98.0%

: 108-24-7
acetic anhydride

: 157727-66-7
1L-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

: 166184-27-6
1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Guidance literature:: With pyridine;
DOI:10.1039/c39940001495

Reference yield:

: 6848-53-9
L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol

: 166184-27-6
1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / dimethylformamide

2: 70 percent / p-TSA, HOCH₂CH₂OH / CH₂Cl₂

3: 98 percent / pyridine

With pyridine; toluene-4-sulfonic acid; ethylene glycol; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c39940001495

Reference yield:

: 100-39-0
benzyl bromide

: 166184-27-6
1L-3,4-di-O-acetyl-1-O-benzyl-5,6-O-cyclohexylidene-2-O-methyl-chiro-inositol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / dimethylformamide

2: 70 percent / p-TSA, HOCH₂CH₂OH / CH₂Cl₂

3: 98 percent / pyridine

With pyridine; toluene-4-sulfonic acid; ethylene glycol; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c39940001495