2,3,5-TRI-O-BENZYL-1,4-DIDEOXY-1,4-[[(2R,3R)-2,4-O-BENZYLIDENE-3-(SULFOOXY)-BUTYL]-EPISULFONIUMYLIDENE]-D-ARABINITOL-INNER-SALT
Compound with spectra: 1 NMR
![2,3,5-TRI-O-BENZYL-1,4-DIDEOXY-1,4-[[(2R,3R)-2,4-O-BENZYLIDENE-3-(SULFOOXY)-BUTYL]-EPISULFONIUMYLIDENE]-D-ARABINITOL-INNER-SALT](/api/compound/TnIMwFrJhO.png?ph=true&h=300&w=458 "2,3,5-TRI-O-BENZYL-1,4-DIDEOXY-1,4-[[(2R,3R)-2,4-O-BENZYLIDENE-3-(SULFOOXY)-BUTYL]-EPISULFONIUMYLIDENE]-D-ARABINITOL-INNER-SALT")
| SpectraBase Compound ID | TnIMwFrJhO |
|---|---|
| InChI | InChI=1S/C37H40O9S2/c38-48(39,40)46-32-24-44-37(31-19-11-4-12-20-31)45-33(32)26-47-27-34(42-22-29-15-7-2-8-16-29)36(43-23-30-17-9-3-10-18-30)35(47)25-41-21-28-13-5-1-6-14-28/h1-20,32-37H,21-27H2/t32-,33+,34+,35+,36-,37?,47?/m0/s1 |
| InChIKey | ZTEWTEIDCJSDNM-FVLGLQIASA-N |
| Mol Weight | 692.8 g/mol |
| Molecular Formula | C37H40O9S2 |
| Exact Mass | 692.211375 g/mol |
| Enantiomer InChIKey | ZTEWTEIDCJSDNM-QUSULMHRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD2Cl2 |
2,3,5-TRI-O-BENZYL-1,4-DIDEOXY-1,4-[[(2S,3S)-2,4-BENZYLIDENEDIOXY-3-(SULFOXY)-BUTYL]-EPISELENONIUMYLIDENE]-D-ARABINITOL-INNER-SALT
2,3,5-TRI-O-BENZYL-1,4-DIDEOXY-1,4-[[(2R,3R)-2,4-BENZYLIDENEDIOXY-3-(SULFOXY)-BUTYL]-EPISELENONIUMYLIDENE]-D-ARABINITOL-INNER-SALT
1-(METHYL-2-O-BENZYL-4,6-O-BENZYLIDENE-3-DEOXY-ALPHA-D-ALTROPYRANOSID-3-YL)-BUT-3-YN-2-ONE
O-(2,3,4,6-Tetra-O-benzyl-d-glucopyranosyl)-N,N-bis-(2-chloroethyl)-phosphordiamidate
4-O-(2,3,4,6-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSYL)-2,3,6-TRI-O-BENZYL-ALPHA-D-GLUCOPYRANOSIDE
METHYL-4,6-O-BENZYLIDENE-3-O-PARA-TOLUENESULFONYL-BETA-D-GALACTOSIDE
Methyl 4,6-O-benzylidene-3-O-tosyl-.alpha.,D-mannopyranoside
2-O-(2,3,5-TRI-O-BENZOYL-BETA-D-RIBOFURANOSYL)-1,3,4-TRI-O-BENZYL-5-O-PIVALOYL-D-RIBITOL
| Title | Journal or Book | Year |
|---|---|---|
| A New Class of Glycosidase Inhibitor: Synthesis of Salacinol and Its Stereoisomers | The Journal of Organic Chemistry | 2001 |