4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside
CAS No.:1135552-11-2
Molecular Formula:C₃₄H₂₈F₂O₇S
Molecular Weight:618.655
Hs Code.:

Synonyms:4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

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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 4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

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Technology Process of 4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

There total 1 articles about 4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 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: 100.0%

: 403-43-0
4-fluorobenzoyl chloride

: 219518-19-1
4-methylphenyl 4,6-O-benzylidene-1-thio-β-D-glucopyranoside

: 1135552-11-2
4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1002/ejoc.200800670

Reference yield: 57.0%

: 1135552-11-2
4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

: C₃₃H₅₃FN₅O₉Pol

: C₆₀H₇₃F₃N₅O₁₆Pol

Guidance literature:: 4-methylphenyl 2,3-di-O-(4-fluorobenzoyl)-4,6-O-benzylidene-1-thio-β-D-glucopyranoside; C₃₃H₅₃FN₅O₉Pol; With tetrabutylammonium trifluoromethylsulfonate; In dichloromethane; for 0.166667h; Molecular sieve; solid phase reaction;

With N-Bromosuccinimide; In dichloromethane; at 20 ℃; Darkness; Molecular sieve; solid phase reaction;
DOI:10.1002/ejoc.200800670