sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

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Chemical Name:sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate
CAS No.:1209013-00-2
Molecular Formula:C₂₉H₂₇ClF₂N₃O₁₂S*Na
Molecular Weight:738.052
Hs Code.:

sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

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Chemical Property of sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

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Technology Process of sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

There total 1 articles about sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate 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: 40.0%

: 1209012-97-4
methyl ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-4,7,8-tri-O-acetyl-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

: 1209013-00-2
sodium ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate

Guidance literature:: methyl ((2,3-difluorobenzyl) 5-(o-nitrotoluenesulfonamido)-4,7,8-tri-O-acetyl-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate; With water; lithium hydroxide; In tetrahydrofuran;

DOI:10.1021/jm901517k