(2S,3R)-3-Phenylglutamic acid
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Ld6f4IpCceJ |
|---|---|
| InChI | InChI=1S/C11H13NO4/c12-10(11(15)16)8(6-9(13)14)7-4-2-1-3-5-7/h1-5,8,10H,6,12H2,(H,13,14)(H,15,16)/t8-,10-/m0/s1 |
| InChIKey | UXEDFOHTFRNIJS-WPRPVWTQSA-N |
| Mol Weight | 223.23 g/mol |
| Molecular Formula | C11H13NO4 |
| Exact Mass | 223.084458 g/mol |
| Enantiomer InChIKey | UXEDFOHTFRNIJS-PSASIEDQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
(2R,3S)-3-Phenylglutamic acid hydrochloride
Glutaric acid, 2-methyl-3-phenyl-
2-AMINO-3-PHENYL-4,4,4-TRIFLUOROBUTYRIC ACID (DIASTEREOMER MIXTURE)
(1-PHENYLBUTYL)-PROPANEDIOIC_ACID
2-amino-3-(4-nitrophenyl)butanoic acid
Ethyl 4,4-Dicyano-3-phenylbutyrate
TRANS-5-METHYL-4-PHENYL-4,5-DIHYDRO-2(3H)-FURANONE
(3R,4S)-3-Methyl-4-phenyl-pyrrolidin-2-one
cis-3-Methyl-4-phenyl-2-pyrolidinone
Phenibut 2TMS
| 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 |
Wiley Registry of Mass Spectral Data 12th Edition
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