2-[BOC-NH-L-TRYPTOPHANAMIDO-(2-ETHOXY)]-ETHYL-(PARA-CHLOROPHENYL)-PHOSPHATE
Compound with spectra: 1 NMR
![2-[BOC-NH-L-TRYPTOPHANAMIDO-(2-ETHOXY)]-ETHYL-(PARA-CHLOROPHENYL)-PHOSPHATE](/api/compound/IseXdrnuwaq.png?ph=true&h=300&w=458 "2-[BOC-NH-L-TRYPTOPHANAMIDO-(2-ETHOXY)]-ETHYL-(PARA-CHLOROPHENYL)-PHOSPHATE")
| SpectraBase Compound ID | IseXdrnuwaq |
|---|---|
| InChI | InChI=1S/C26H33ClN3O8P/c1-26(2,3)37-25(32)30-23(16-18-17-29-22-7-5-4-6-21(18)22)24(31)28-12-13-35-14-15-36-39(33,34)38-20-10-8-19(27)9-11-20/h4-11,17,23,29H,12-16H2,1-3H3,(H,28,31)(H,30,32)(H,33,34)/t23-/m0/s1 |
| InChIKey | MDLCKKQHTKMTIQ-QHCPKHFHSA-N |
| Mol Weight | 582.0 g/mol |
| Molecular Formula | C26H33ClN3O8P |
| Exact Mass | 581.16938 g/mol |
| Enantiomer InChIKey | MDLCKKQHTKMTIQ-HSZRJFAPSA-N |
| Racemate InChIKey | MDLCKKQHTKMTIQ-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O:CD3OD |
2-[TRIFLUOROACETAMIDO-NH-L-TRYPTOPHANAMIDO-(2-ETHOXY)]-ETHYL-(PARA-CHLOROPHENYL)-PHOSPHATE
benzyl (1R)-2-{[(1S)-1-(aminocarbonyl)-3-methylbutyl]amino}-1-(1H-indol-3-ylmethyl)-2-oxoethylcarbamate
2-Methylpropyl N-[3-(1H-indol-3-yl)-1-[(4-methyl-1,3-thiazol-2-yl)amino]-1-oxidanylidene-propan-2-yl]carbamate
N-{1-(1H-indol-3-ylmethyl)-2-oxo-2-[(2-pyridinylmethyl)amino]ethyl}-4-methylcyclohexanecarboxamide
2-{[(cyclohexylamino)carbonyl]amino}-3-(1H-indol-3-yl)-N-(4-methoxyphenyl)propanamide
Butyl 2-([2-(acetylamino)-3-(1H-indol-3-yl)propanoyl]amino)-4-methylpentanoate
Cyclo-(D-ile-L-trp)
L-Leucine, N-[N-(N-acetyl-L-alanyl)-L-tryptophyl]-
L-Alanine, N-[N-[N-[N-(1-oxodecyl)glycyl]-L-tryptophyl]-L-alanyl]-, methyl ester
1H-indole-3-propanamide, alpha-[[(4-methylcyclohexyl)carbonyl]amino]-N-(2-pyridinyl)-
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of nucleotide–amino acid conjugates designed for photo-CIDNP experiments by a phosphotriester approach | Beilstein Journal of Organic Chemistry | 2013 |