N-TERT.-BUTOXYCARBONYL-L-GLUTAMIC-ACID-ALPHA-TERT.-BUTYLESTER-GAMMA-N-METHOXY-N-METHYLAMIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 86A5kyFsrea |
|---|---|
| InChI | InChI=1S/C16H30N2O6/c1-15(2,3)23-13(20)11(9-10-12(19)18(7)22-8)17-14(21)24-16(4,5)6/h11H,9-10H2,1-8H3,(H,17,21)/t11-/m0/s1 |
| InChIKey | KZYLEOANPQRWKH-NSHDSACASA-N |
| Mol Weight | 346.42 g/mol |
| Molecular Formula | C16H30N2O6 |
| Exact Mass | 346.210387 g/mol |
| Enantiomer InChIKey | KZYLEOANPQRWKH-LLVKDONJSA-N |
| Racemate InChIKey | KZYLEOANPQRWKH-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-TERT.-BUTOXYCARBONYL-L-GLUTAMIC-ACID-GAMMA-BENZYL-ALPHA-TERT.-BUTYL-DIESTER
BENZYL-[(2R)-N-(TERT.-BUTOXYCARBONYL)-ALPHA-METHYLGLUTAMYL]-GAMMA-GLYCINATE-DIESTER
1-TERT.-BUTYL-(2S,4S)-N-(TERT.-BUTOXYCARBONYL)-4-METHYLGLUTAMIC_ACID
TERT.-BUTYL-N-(TERT.-BUTOXYCARBONYL)-5-NITRO-4-OXO-L-NORVALINATE
TERT.-BUTYL-(2S,4S)-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-4-HYDROXY-5-NITRO-BUTANOATE
TERT.-BUTYL-(2S,4R)-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-4-HYDROXY-5-NITRO-BUTANOATE
N-Benzyloxycarbonyl-L-glutamic acid 1-tert-butyl ester dicyclohexylammonium salt
tert-Butyl 4-(N-acetyl-S-methylsulfinimidoyl)-2-[(tert-butoxycarbonyl)amino]butanoate
TERT.-BUTYL-(2S)-2-(TERT.-BUTYLOXYCARBONYLAMINO)-4-(DIMETHYLPHOSPHONO)-BUTANOATE
TERT.-BUTYL-2-(TERT.-BUTOXYCARBONYLAMINO)-5-CYANO-4,4-DIDEUTERIOPENTANOATE
| Title | Journal or Book | Year |
|---|---|---|
| The synthesis of pyrimidin-4-yl substituted α-amino acids. A versatile approach from alkynyl ketones | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
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.