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Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate

Compound with spectra: 3 NMR

Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate
SpectraBase Compound ID 2Evx2Axd7rV
InChI InChI=1S/C18H28ClN3O5/c1-12(18(26)27-2)20-16(24)13-6-4-11-22(13)17(25)14-7-5-10-21(14)15(23)8-3-9-19/h12-14H,3-11H2,1-2H3,(H,20,24)/t12-,13+,14+/m1/s1
InChIKey KYOGGPLOZCMDBI-RDBSUJKOSA-N
Mol Weight 401.89 g/mol
Molecular Formula C18H28ClN3O5
Exact Mass 401.171749 g/mol
Enantiomer InChIKey KYOGGPLOZCMDBI-BFHYXJOUSA-N

View Spectrum of Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate
N-Tfa-L-prolylproline butyl ester
(3S,6R)-6-Allyl-1-(2,2-diethoxyethyl)-3,4-propylidene-1,4-piperazine-2,5-dione
L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER-HYDROTRIFLUOROACETATE
Cyclo(leucylprolyl),AC
Cyclo-(glycyl-L-prolyl-L-seryl-D-alanyl-L-prolyl)
Alanine, N-[N-[N-[1-(4-bromobenzoyl)-L-prolyl]-L-valyl]-2-methylalanyl]-2-methyl-, methyl ester
Alanine, N-[N-[N-[1-(4-chlorobenzoyl)-L-prolyl]-L-valyl]-2-methylalanyl]-2-methyl-, methyl ester
L-Valine, N-[N-(1-alloisoleucyl-L-prolyl)-N-methylglycyl]-N-methyl-, methyl ester
TERT-BUTYLOXYCARBONYL-[N(OMEGA)-NITRO]ARGININ-[N(OMEGA)-NITRO]ARGININ-PROLIN METHYL ESTER TRIPEPTIDE
METHYL-N-(BENZYLOXYCARBONYL)-GLYCYLPROLYLPHENYLALANYLPHENYLALANINE
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
Methyl (2S)-N-[(2S)-N-[(2S)-N-(4-chlorobutyryl)prolyl]prolyl}alaninate
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