(2S,3S)-3-METHYLPYROGLUTAMIC-ACID
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 9tkVKAP7Md9 |
|---|---|
| InChI | InChI=1S/C6H9NO3/c1-3-2-4(8)7-5(3)6(9)10/h3,5H,2H2,1H3,(H,7,8)(H,9,10)/t3-,5-/m0/s1 |
| InChIKey | HPCPEJXLESDEDM-UCORVYFPSA-N |
| Mol Weight | 143.14 g/mol |
| Molecular Formula | C6H9NO3 |
| Exact Mass | 143.058243 g/mol |
| Enantiomer InChIKey | HPCPEJXLESDEDM-NQXXGFSBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(2R*,3R*)-2-ACETAMIDO-3-METHYLPENTANOIC-ACID;(2R*,3R*)-N-ACETYL-DL-ISOLEUCINE
D-Alloisoleucine, N-acetyl-
(2R*,3S*)-2-ACETAMIDO-3-METHYLPENTANOIC-ACID;(2R*,3S*)-N-ACETYL-DL-ALLOISOLEUCINE
L-Valine, N-(1-oxopentyl)-
N-GLYCYL-L-THREONINE
N-glycyl-DL-threonine
N-GLYCYL-D-THREONINE
D-Valine, N-(chloroacetyl)-, methyl ester
Glycyl-leucine cation
| Title | Journal or Book | Year |
|---|---|---|
| Michael Addition Reactions between Chiral Ni(II) Complex of Glycine and 3-(trans-Enoyl)oxazolidin-2-ones. A Case of Electron Donor−Acceptor Attractive Interaction-Controlled Face Diastereoselectivity1 | The Journal of Organic Chemistry | 2001 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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