FMOC-ALA-ALA-CH2CL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 7JEnsBmWpvM |
|---|---|
| InChI | InChI=1S/C22H23ClN2O4/c1-13(20(26)11-23)24-21(27)14(2)25-22(28)29-12-19-17-9-5-3-7-15(17)16-8-4-6-10-18(16)19/h3-10,13-14,19H,11-12H2,1-2H3,(H,24,27)(H,25,28)/t13-,14+/m1/s1 |
| InChIKey | XFDOLUIIHJTPTB-KGLIPLIRSA-N |
| Mol Weight | 414.89 g/mol |
| Molecular Formula | C22H23ClN2O4 |
| Exact Mass | 414.134635 g/mol |
| Enantiomer InChIKey | XFDOLUIIHJTPTB-UONOGXRCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
FMOC-ALA-ALA-ME
CYS-03-INTERMEDIATE
N-{[N'-(Fluorenyl)methoxycarbonyl]-serinyl}-.beta.-alanine
Fmoc-Met(O)-OH
FMOC-S-Acetamidomethyl-L-cysteine
L-3-(tert-BUTYLDITHIO)-N-CARBOXYALANINE, N-[(FLUOREN-9-YL)METHYL]ESTER
N-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-S-tert-butyl-L-cysteine
METHYL-2-(FLUOREN-9-YL-METHOXYCARBONYLAMINO)-HEX-5-ENOATE
Nε-Allyloxycarbonyl-Nα-(9-fluorenylmethyloxycarbonyl)-D-lysine
Nα-(9-Fluorenylmethoxycarbonyl)-L-arginine
| 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.