C₅₅H₅₆O₁₂S

Base Information

Chemical Name:C₅₅H₅₆O₁₂S
CAS No.:1093383-85-7
Molecular Formula:C₅₅H₅₆O₁₂S
Molecular Weight:941.108
Hs Code.:

C<sub>55</sub>H<sub>56</sub>O<sub>12</sub>S

Synonyms:C₅₅H₅₆O₁₂S

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Chemical Property of C₅₅H₅₆O₁₂S

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Technology Process of C₅₅H₅₆O₁₂S

There total 2 articles about C₅₅H₅₆O₁₂S 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: 65.0%

: 1093383-69-7
C₂₇H₂₈O₆S

: C₃₆H₃₆O₉

: 1093383-85-7
C₅₅H₅₆O₁₂S

Guidance literature:: With 2,6-di-tert-butyl-4-methylpyridine; trifluoromethylsulfonic anhydride; In dichloromethane; at -60 - 0 ℃; stereoselective reaction; Molecular sieve;
DOI:10.1021/jo8020192

Reference yield: 43.0%

: methyl (phenyl 2,3,4-tri-O-benzyl-1-thio-α-D-mannopyranoside)uronate

: 1093383-69-7
C₂₇H₂₈O₆S

: 1093383-85-7
C₅₅H₅₆O₁₂S

Guidance literature:: methyl (phenyl 2,3,4-tri-O-benzyl-1-thio-α-D-mannopyranoside)uronate; With trifluoromethylsulfonic anhydride; 1,1'-sulfinylbisbenzene; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; at -60 - -45 ℃; for 0.25h; Molecular sieve;

C₂₇H₂₈O₆S; In dichloromethane; at -60 - 0 ℃; stereoselective reaction;
DOI:10.1021/jo8020192

Reference yield: 74.0%

: C₂₄H₂₉N₃O₇

: 1093383-85-7
C₅₅H₅₆O₁₂S

: 1093383-89-1
C₇₃H₇₉N₃O₁₉

Guidance literature:: C₅₅H₅₆O₁₂S; With 1-benzenesulfinyl piperidine; trifluoromethylsulfonic anhydride; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; at -60 - -45 ℃; for 0.25h; Molecular sieve;

C₂₄H₂₉N₃O₇; In dichloromethane; at -60 - 0 ℃; stereoselective reaction;
DOI:10.1021/jo8020192