(2S,3S,4R,5S,6S)-METHYL-3''-[1'-[3,5-DIHYDROXY-2,6-BIS-(HYDROXYMETHYL)-7,7-DIMETHYL-OXEPAN-4-YL]-1H-1',2',3'-(TRIAZOL-4'-YL)]-3''-METHYLBUTANOATE
Compound with spectra: 1 NMR
![(2S,3S,4R,5S,6S)-METHYL-3''-[1'-[3,5-DIHYDROXY-2,6-BIS-(HYDROXYMETHYL)-7,7-DIMETHYL-OXEPAN-4-YL]-1H-1',2',3'-(TRIAZOL-4'-YL)]-3''-METHYLBUTANOATE](/api/compound/110tBqn07Mx.png?ph=true&h=300&w=458 "(2S,3S,4R,5S,6S)-METHYL-3''-[1'-[3,5-DIHYDROXY-2,6-BIS-(HYDROXYMETHYL)-7,7-DIMETHYL-OXEPAN-4-YL]-1H-1',2',3'-(TRIAZOL-4'-YL)]-3''-METHYLBUTANOATE")
| SpectraBase Compound ID | 110tBqn07Mx |
|---|---|
| InChI | InChI=1S/C18H31N3O7/c1-17(2,6-13(24)27-5)12-7-21(20-19-12)14-15(25)10(8-22)18(3,4)28-11(9-23)16(14)26/h7,10-11,14-16,22-23,25-26H,6,8-9H2,1-5H3/t10-,11-,14+,15-,16+/m0/s1 |
| InChIKey | JINHATAMVDURAJ-APVVIDPYSA-N |
| Mol Weight | 401.46 g/mol |
| Molecular Formula | C18H31N3O7 |
| Exact Mass | 401.2162 g/mol |
| Enantiomer InChIKey | JINHATAMVDURAJ-HTUPGXDSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD:CDCl3 |
PKKPWWDZCMACJH-AOJJOOHFSA-N
UTNYALQLQFDRKE-FZGYHVDVSA-N
Tetrahydro-3-hydroxy-4-[(2R-trans)-1,6-dimethyl-2-oxo-cyclohexyl]-[4R(4alpha(R*),3zeta)]-furan-2-carboxylic acid methyl ester
Cocaine-M (HO-methoxy-) PFP
LINCOMYCIN-SULFONE
FYKWXCCLFISIOS-CTEUCUGASA-N
MEEHANINE_I;ISOMER_1
11,13-Dihydro-13-methoxysesquiterpene lactone
4-[(3-CHLOROBENZOYL)-AMINO]-4,5-DIDEOXY-N-((1'S)-1'-[(3''S)-3'',4''-DIHYDRO-8''-HYDROXY-1''-OXO-1''H-2''-BENZOPYRAN-3''-YL]-3'-METHYLBUTYL)-ALPHA-D-RIBO-HEXAR-
(2S)-N-[(Fluoren-9'-yl)methoxycarbonyl]phenylalanine prop-2-enyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Di‐ and Trivalent Carbohydrate Mimetics with Oxepane Substructure by Employing Copper‐Catalyzed [3+2] Cycloadditions of Alkynes with Azidooxepanes | European Journal of Organic Chemistry | 2014 |