GAMMA-O-METHYL-GLUTAMYL-N-CARBOXYANHYDRIDE
Compound with spectra: 5 NMR
| SpectraBase Compound ID | 5fSPzsgkmRw |
|---|---|
| InChI | InChI=1S/C7H9NO5/c1-12-5(9)3-2-4-6(10)13-7(11)8-4/h4H,2-3H2,1H3,(H,8,11) |
| InChIKey | JRZZMWDRALHNFH-UHFFFAOYSA-N |
| Mol Weight | 187.15 g/mol |
| Molecular Formula | C7H9NO5 |
| Exact Mass | 187.048072 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CF3COOH |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CF3COOH |
- 3-(4-Oxazolidine-2,5-dione)-propanoic acid, methyl ester
N-(tert-Butoxycarbonyl)-L-glutamic acid
N-(tert-Butoxycarbonyl)-D-glutamic acid
METHYL-(S)-2-TERT.-BUTOXYCARBONYLAMINO-5-HYDROXY-NORVALINATE
Boc-Gln-OH
L-4-(carboxyamino)glutaramic acid, N-tert-butyl ester
(S)-N-ALPHA-TERT.-BUTOXYCARBONYLGLUTAMINEAMIDE
Methyl (2S)-2-(ethoxycarbonylamino)heptanoate
Methyl (2S)-2-(ethoxycarbonylamino)octanoate
(S)-2-tert-Butoxycarbonylamino-hex-5-enoic acid methyl ester
Methyl (2R)-2-(tert-Butoxycarbonylamino)-5-hexenoate
| Title | Journal or Book | Year |
|---|---|---|
| 15N NMR spectroscopy 24—chemical shifts and coupling constants of α-amino acidN-carboxyanhydrides and related heterocycles | Organic Magnetic Resonance | 1980 |
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.