1-(4-amino-3-nitrophenyl)ethanone

CC(NS(=O)C(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #192115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(N)c([N+](=O)[O-])c1
Reaction #277638
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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Reaction #642604
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(=O)c1ccc(N)c([N+](=O)[O-])c1
Reaction #669093
4-Acetyl-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC(=O)c1ccc(Nc2cccc(Br)c2)c([N+](=O)[O-])c1
Reaction #669094
N-(3-Bromophenyl)-4-acetyl-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC(=O)c1ccc(N)c([N+](=O)[O-])c1
Reaction #669144
4-Acetyl-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC(=O)c1ccc(Nc2cccc(Br)c2)c([N+](=O)[O-])c1
Reaction #669145
N-(3-bromophenyl)-4-acetyl-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC(NS(=O)C(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #1181817
title compound
Rendimiento 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CC(NS(=O)C(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #2196020
title compound
Rendimiento 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
CC(=O)c1ccc(N)c(N)c1
Reaction #2399035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
CC(=O)c1ccc(N)c(N)c1
Reaction #2464996
142a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12