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TRANS-[3-(13)-C,(14)-C]-CINNAMIC-ACID-N-ACETYL-CYSTEAMINE-THIOESTER

Compound with spectra: 1 NMR

TRANS-[3-(13)-C,(14)-C]-CINNAMIC-ACID-N-ACETYL-CYSTEAMINE-THIOESTER
SpectraBase Compound ID 3S11eL9bM5j
InChI InChI=1S/C13H15NO2S/c1-11(15)14-9-10-17-13(16)8-7-12-5-3-2-4-6-12/h2-8H,9-10H2,1H3,(H,14,15)/b8-7+/i7+1
InChIKey UFDKNYAHUYGCIC-WRFSBCFPSA-N
Mol Weight 250.32 g/mol
Molecular Formula C1213CH15NO2S
Exact Mass 250.085705 g/mol

View Spectrum of TRANS-[3-(13)-C,(14)-C]-CINNAMIC-ACID-N-ACETYL-CYSTEAMINE-THIOESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(r)-3-Hydroxy-5-oxohexanoic acid - (S)-[2'-(Acetylamino)ethyl] Thioester
(S)-3-Hydroxy-5-oxohexanoic acid - (S)-[2'-(Acetylamino)ethyl] Thioester
N-Acetylcystemine (S)-[2,3-13C2]-7-hydroxyoctanoate
(2,3-13C2)-3-KETOHEXANOIC-ACID-N-ACETYLCYSTEAMINEESTER
N-TRIFLUOROACETYL-ETHYL-PHENYLSULFILIMINE
2-mercaptoacetanilide, acetate
N.N'-bis(benzylthioethyl)malonamide
Carbamic acid, (thiodiethylene)di-, dibenzyl ester
Butanethioic acid, S-3-hydroxy-2-octanamidoethyl ester
Benzoylthiocholine iodide
Title Journal or Book Year
Biosynthesis of the benzoyl moiety of cocaine from cinnamic acid via (R)-(+)-3-hydroxy-3-phenylpropanoic acid Phytochemistry 1992
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