Methyl (2S)-N-[(2S)-N-(tert-butoxycarbonyl)prolyl]alaninate
Compound with spectra: 1 NMR, and 1 MS (GC)
![Methyl (2S)-N-[(2S)-N-(tert-butoxycarbonyl)prolyl]alaninate](/api/compound/KvmzFgjLooJ.png?ph=true&h=300&w=458 "Methyl (2S)-N-[(2S)-N-(tert-butoxycarbonyl)prolyl]alaninate")
| SpectraBase Compound ID | KvmzFgjLooJ |
|---|---|
| InChI | InChI=1S/C14H24N2O5/c1-9(12(18)20-5)15-11(17)10-7-6-8-16(10)13(19)21-14(2,3)4/h9-10H,6-8H2,1-5H3,(H,15,17)/t9-,10-/m0/s1 |
| InChIKey | QIEXZZYYAOKYCI-UWVGGRQHSA-N |
| Mol Weight | 300.36 g/mol |
| Molecular Formula | C14H24N2O5 |
| Exact Mass | 300.168522 g/mol |
| Enantiomer InChIKey | QIEXZZYYAOKYCI-NXEZZACHSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | KC-0-3773-15 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
tert-Butyl 2-[(4-bromoanilino)carbonyl]-1-pyrrolidinecarboxylate
Pyrrolidine-1-carboxylic acid, 2-cycloheptylaminocarbonyl-, benzyl ester
GLYCINE-PROLINE-ALANINE-GLYCINE-ALANINE-GLYCINE
GLYCINE-PROLINE-D-ALANINE-GLYCINE-ALANINE-GLYCINE
isobutyl 2-[(4-methoxyanilino)carbonyl]-1-pyrrolidinecarboxylate
(S)-N-(Benzyloxycarbonyl)prolinanilide
2-benzyl-3-oxo-1-piperazinecarboxylic acid, tert-butyl ester
1-Acetyl -2-[N-(2-hydroxy-1-(methylcarbamoyl)propyl)carbamyl]pyrrolidine
N-{[1'-(t-Butoxycarbonyl)-2'-pyrrolidinyl] - methyl-D-phenylalanine - methyl ester
N-{[1'-(t-Butoxycarbonyl)-2'-pyrrolidinyl] - methyl-L-phenylalanine - methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Design, construction and properties of peptide N-terminal cap templates devised to initiate α-helices. Part 1. Caps derived from N-(4-chlorobutyryl)-(2S )-Pro-(2S )-Pro-(2S )-Ala-OMe and N-[(2S )-2-chloropropionyl]-(2S )-Pro-(2S )-Pro-(2S,4S )-4-hydroxyPro-OMe | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |