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[2-(4-NITROPHENYL-[N15]-ETHYLAMINO]-[13C2]-OXOACETIC-ACID

Compound with spectra: 2 NMR

[2-(4-NITROPHENYL-[N15]-ETHYLAMINO]-[13C2]-OXOACETIC-ACID
SpectraBase Compound ID 6uvDCLXbgsP
InChI InChI=1S/C10H10N2O5/c13-9(10(14)15)11-6-5-7-1-3-8(4-2-7)12(16)17/h1-4H,5-6H2,(H,11,13)(H,14,15)/i9+1,10+1,11+1
InChIKey UEWDDROENRBSFO-PCBKLFQUSA-N
Mol Weight 241.18 g/mol
Molecular Formula C813C2H10N15NO5
Exact Mass 241.062716 g/mol

View Spectrum of [2-(4-NITROPHENYL-[N15]-ETHYLAMINO]-[13C2]-OXOACETIC-ACID

15N NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of [2-(4-NITROPHENYL-[N15]-ETHYLAMINO]-[13C2]-OXOACETIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
N,N-Dimethyl-p-nitrobenzepropanamide
Benzenebutanoic acid, 4-nitro-, methyl ester
Ethyl 3-(4-nitrophenyl)propanoate
1-(4-Nitrophenyl)octan-3-one
1-(2-benzoxyethyl)-4-nitro-benzene
TVCHABDWNZPZJC-UHFFFAOYSA-N
Benzeneethanamine, N-methyl-4-nitro-N-(2-phenylethyl)-
Methyl (E)-3-[2-(4-Nitrophenyl)ethoxy]acrylate
1-(4-Nitro-phenethyl)-pyridinium cation
1-(cyclopentylmethyl)-4-nitro-benzene
Title Journal or Book Year
Synthesis of13C,15N-enriched α-dicarbonyl model adducts to determine the utility of13c and15N NMR for studying mechanism-based inactivation of cytochromes P-450 by substituted dichloroacetamides Magnetic Resonance in Chemistry 1994
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