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5-AMINO-[1,4-(C-13)2]-LAEVULINIC-ACID-HYDROCHLORIDE

Compound with spectra: 1 NMR

5-AMINO-[1,4-(C-13)2]-LAEVULINIC-ACID-HYDROCHLORIDE
SpectraBase Compound ID HQtzvP53JZ8
InChI InChI=1S/C5H9NO3.ClH/c6-3-4(7)1-2-5(8)9;/h1-3,6H2,(H,8,9);1H/p-1/i4+1,5+1;
InChIKey ZLHFONARZHCSET-BIZAMFJHSA-M
Mol Weight 168.57 g/mol
Molecular Formula C313C2H9ClNO3
Exact Mass 168.033806 g/mol
Parent InChIKey ZGXJTSGNIOSYLO-MQIHXRCWSA-M

View Spectrum of 5-AMINO-[1,4-(C-13)2]-LAEVULINIC-ACID-HYDROCHLORIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Sodium butyrate-1-13C
[1-13C,1602]-SODIUM-HEXANOATE
Octanoic acid-1-13C
DL-Alanine-1-13C
(R,S)-[1-13C]-BETA-AMINOISOBUTYRATE
SODIUM-[1-13C,3,3,3-2H3]-PROPIONATE
Propanedioic-1,3-13C2 acid
SODIUM-[1-13C]-METHYLACRYLATE
2-Bromopropionic acid-1-13C
1-(13)-C-SODIUM-LACTATE
Title Journal or Book Year
Biosynthesis of porphyrins and related macrocycles. Part 41. Fate of oxygen atoms as precorrin-2 carrying eight labelled carboxyl groups (13C18O2H) is enzymatically converted into cobyrinic acid Journal of the Chemical Society, Perkin Transactions 1 1993
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