(2S)-N-{(2S)-N-[(2S)-2-Chloropropionyl]prolyl}proline
Compound with spectra: 1 NMR, and 1 MS (GC)
![(2S)-N-{(2S)-N-[(2S)-2-Chloropropionyl]prolyl}proline](/api/compound/IMrcxVN1Ynb.png?ph=true&h=300&w=458 "(2S)-N-{(2S)-N-[(2S)-2-Chloropropionyl]prolyl}proline")
| SpectraBase Compound ID | IMrcxVN1Ynb |
|---|---|
| InChI | InChI=1S/C13H19ClN2O4/c1-8(14)11(17)15-6-2-4-9(15)12(18)16-7-3-5-10(16)13(19)20/h8-10H,2-7H2,1H3,(H,19,20)/t8-,9-,10-/m0/s1 |
| InChIKey | VIUYPHUBQNROPQ-GUBZILKMSA-N |
| Mol Weight | 302.76 g/mol |
| Molecular Formula | C13H19ClN2O4 |
| Exact Mass | 302.103335 g/mol |
| Enantiomer InChIKey | VIUYPHUBQNROPQ-OPRDCNLKSA-N |
| Copyright | Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | KC-0-3774-20 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- (2S)-1-[(2S)-1-[(2S)-2-chloranylpropanoyl]pyrrolidin-2-yl]carbonylpyrrolidine-2-carboxylic acid
- (2S)-1-[(2S)-1-[(2S)-2-chloropropanoyl]pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid
- (2S)-1-({(2S)-1-[(2S)-2-chloropropanoyl]pyrrolidinyl}carbonyl)-2-pyrrolidinecarboxylic acid
- (2S)-1-[[(2S)-1-[(2S)-2-chloro-1-oxopropyl]-2-pyrrolidinyl]-oxomethyl]-2-pyrrolidinecarboxylic acid
3-Methyl-1,4-diazabicyclo[4.3.0]nonan-2,5-dione, N-acetyl-
2-Pyrrolidineacetic acid, 1-[[1-(trifluoroacetyl)-2-pyrrolidinyl]carbonyl]-, methyl ester, [S-(R*,R*)]-
4-PHENYL-BUTANONOIC-ACID-DERIVATE-OF-LISINOPRIL
N-TERT.-BUTYLOXYCARBONYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLINE
2-[[2-[acetyl(methyl)amino]-5-[(4,6-dimethyl-2-pyrimidinyl)-methylamino]-1-oxopentyl]-methylamino]-5-[(4,6-dimethyl-2-pyrimidinyl)-methylamino]pentanoic acid methyl ester
Leucyl-arginyl-prolyl-glycyl-amide
Methcathinone TPC Derivative
2-[3-[4-(META-NITROPHENYL)-PIPERAZIN-1-YL]-PROPYL]-1,4-DIOXOPERHYDRO-PYRROLO-[1,2-A]-PYRAZINE
Butyl N-(N-acetylphenylalanyl)-1-pyrrolidinecarboxylate
N-[(RS)-(1,1-DIOXO-1,2-THIAZETIDINE-3-YL)-ACETYL]-L-ALANYL-L-PROLINE_BENZYLESTER
| 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 |
This compound is available in the following databases:
KnowItAll GC-MS Library
Author: Wiley
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Wiley Registry of Mass Spectral Data 2026
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.