FMOC-ALA-ALA-ME
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 68YbxA1X84x |
|---|---|
| InChI | InChI=1S/C22H24N2O4/c1-13(15(3)25)23-21(26)14(2)24-22(27)28-12-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,13-14,20H,12H2,1-3H3,(H,23,26)(H,24,27)/t13-,14+/m1/s1 |
| InChIKey | CRHFSTGUMOSRKZ-KGLIPLIRSA-N |
| Mol Weight | 380.44 g/mol |
| Molecular Formula | C22H24N2O4 |
| Exact Mass | 380.173607 g/mol |
| Enantiomer InChIKey | CRHFSTGUMOSRKZ-UONOGXRCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
FMOC-ALA-ALA-CH2CL
N-{[N'-(Fluorenyl)methoxycarbonyl]-serinyl}-.beta.-alanine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-leucine
N-CARBOXY-L-LEUCINE, N-[(FLUOREN-9-YL)METHYL] ESTER
Fmoc-L-leucine
(S)-N-(9-FLUORENYLMETHYLOXYCARBONYL)-2-AMINO-4-HEXYNOIC-ACID;FMOC-BUG-OH
Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine hydrochloride
FMOC-LYS-OH
Fmoc-Nle-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-threonine
| Title | Journal or Book | Year |
|---|---|---|
| Studies on the Mechanism of 1,2-Dihydropyrazin-2-one Ring Formation from Dipeptidyl Chloromethyl Ketone and Its Chemical Properties: Immediate Deamination during Catalytic Hydrogenation | Chemical and Pharmaceutical Bulletin | 2005 |
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.