LNXAGVSBLXLUAF-UVVOPATOSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | DsLtUtzfKgo |
|---|---|
| InChI | InChI=1S/C25H36N2O8/c1-13(8-21(30)26-11-18(29)16-5-6-22(33-4)27-10-16)7-19-24(32)23(31)17(12-34-19)9-20-25(35-20)14(2)15(3)28/h5-6,8,10,14-15,17,19-20,23-25,28,31-32H,7,9,11-12H2,1-4H3,(H,26,30)/b13-8+/t14-,15+,17-,19-,20+,23+,24-,25-/m1/s1 |
| InChIKey | LNXAGVSBLXLUAF-UVVOPATOSA-N |
| Mol Weight | 492.6 g/mol |
| Molecular Formula | C25H36N2O8 |
| Exact Mass | 492.247166 g/mol |
| Enantiomer InChIKey | LNXAGVSBLXLUAF-YTQVZESZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
MMDKKSZHHRBSHI-XGRSWJMGSA-N
VRVVJOBGGNIYLR-JQKHUKBMSA-N
QDKTUAFNHUPOQK-UVVOPATOSA-N
N-(4-Methylsulfonyl-phenacyl)-monamide
IHRFGVIFKDMCNU-MDWOAMDMSA-N
VZVRJJNBQVGTNU-XPSSKNPZSA-N
N-[(E)-2-(tert-BUTYL-DIMETHYLSILOXYIMINO)-1-PHENYLETHYL]-MONAMIDE
2H-Pyran-3,4-diol, 2-[3-(4,5-dihydro-5-phenyl-2-oxazolyl)-2-methyl-2-propenyl]tetrahydro-5-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-
HGVPNFONYLBHDJ-SZEKAGBESA-N
2H-Pyran-3,4-diol, tetrahydro-5-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-2-[2-methyl-3-(5-phenyl-2-thiazolyl)-2-propenyl]-, [2S-[2.alpha.(E),3.beta.,4.beta.,5.alpha.[2R*,3R*(1R*,2R*)]]]-
| Title | Journal or Book | Year |
|---|---|---|
| The Chemistry of Pseudomonic Acid. Part 14. Synthesis and In Vivo Biological Activity of Heterocyclyl Substituted Oxazole Derivatives. | The Journal of Antibiotics | 1995 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.