2,3,4,5,6-PENTA-O-BENZYL-MYO-INOSITOL-1-[(S)-3,4-DIPALMITOYLOXYBUTYL]-SULFONATE
Compound with spectra: 1 NMR
![2,3,4,5,6-PENTA-O-BENZYL-MYO-INOSITOL-1-[(S)-3,4-DIPALMITOYLOXYBUTYL]-SULFONATE](/api/compound/G3BYrJ1tL1.png?ph=true&h=300&w=458 "2,3,4,5,6-PENTA-O-BENZYL-MYO-INOSITOL-1-[(S)-3,4-DIPALMITOYLOXYBUTYL]-SULFONATE")
| SpectraBase Compound ID | G3BYrJ1tL1 |
|---|---|
| InChI | InChI=1S/C77H110O12S/c1-3-5-7-9-11-13-15-17-19-21-23-25-42-54-70(78)82-63-69(88-71(79)55-43-26-24-22-20-18-16-14-12-10-8-6-4-2)56-57-90(80,81)89-77-75(86-61-67-50-38-30-39-51-67)73(84-59-65-46-34-28-35-47-65)72(83-58-64-44-32-27-33-45-64)74(85-60-66-48-36-29-37-49-66)76(77)87-62-68-52-40-31-41-53-68/h27-41,44-53,69,72-77H,3-26,42-43,54-63H2,1-2H3/t69?,72-,73-,74+,75+,76-,77+ |
| InChIKey | MXASZLJTKMPNMQ-FNHPJLSSSA-N |
| Mol Weight | 1259.8 g/mol |
| Molecular Formula | C77H110O12S |
| Exact Mass | 1258.7718 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
methanesulfonic acid [(2R,3R,4R,5S,6S)-4,5-bis(benzyloxy)-2-methoxy-6-methyl-tetrahydropyran-3-yl] ester
No Name
XXCLPMPANGGIKV-UHFFFAOYSA-N
METHYL-6-O-SULFONATO-2,3,4-TRI-O-BENZYL-ALPHA-D-MANNOPYRANOSIDE
METHYL-6,7-ANHYDRO-2,3-DI-O-BENZYL-8-DEOXY-4-O-METHYL-ALPHA-D-THREO-D-GALACTO-OCTOSIDE
1-O-Benzyl-2-O-methanesulfonyl-3,4:5,6-di-O-isopropylidene-D-glucitol
METHYL-6,7-ANHYDRO-2,3-DI-O-BENZYL-8-DEOXY-ALPHA-D-THREO-D-GLUCO-OCTOPYRANOSIDE
(2R,3S)-Acetic Acid 2-[(Benzyloxy)(2R,3S)-3-(tert-butyldimethylsiloxy)tetrahydropyran-2-yl]-(R)-methyl]tetrahydropyran-3-yl Ester
(1,3-Diazido-prop-2-yl)-2,3,4,6-tetra-O-benzyl-b-d-glucopyranoside
METHYL-3,6-ANHYDRO-2,4-DI-O-BENZYL-L-GLYCERO-BETA-D-MANNO-HEPTOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| An approach toward the synthesis of racemic myo-inositol 1-([S] 3,4-di-palmitoyloxybutyl)-sulfonate | Recueil des Travaux Chimiques des Pays-Bas | 2010 |