BOC-DAP(Z)-CH2CL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 40l28m81QMP |
|---|---|
| InChI | InChI=1S/C17H23ClN2O5/c1-17(2,3)25-16(23)20-13(14(21)9-18)10-19-15(22)24-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,19,22)(H,20,23)/t13-/m0/s1 |
| InChIKey | RJYAQACURRFMIN-ZDUSSCGKSA-N |
| Mol Weight | 370.83 g/mol |
| Molecular Formula | C17H23ClN2O5 |
| Exact Mass | 370.12955 g/mol |
| Enantiomer InChIKey | RJYAQACURRFMIN-CYBMUJFWSA-N |
| Racemate InChIKey | RJYAQACURRFMIN-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
BOC-DAB(Z)-CH2CL
Z-L-Phe chloromethyl ketone
(-)-N-(N-CARBOXY-L-LEUCYL)GLYCINE, N-BENZYL ESTER
Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-leucyl]-, methyl ester
(phenylmethyl) N-[(2S,3S)-2-(hydroxymethyl)-4-oxidanylidene-azetidin-3-yl]carbamate
N-Benzyloxycarbonylglycyl-E-N-(T-butoxycarbonyl)-L-lysine
N-(N-carboxy-D,L-norleucyl)glycine, N-benzyl ester
N-TERT.-BUTYLOXYCARBONYL-O-BENZYL-L-ASPARTIC-ACID
N-Boc-L-aspartic acid 4-benzyl ester
(R,S)-N-BENZYL-2-N-(BENZYLOXYCARBONYL)-2-AMINOPENTANAMIDE
| 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
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