4-nitroaniline

O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccccc1Br
Reaction #5772
2-bromo-N-(4-nitrophenyl)benzamide
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc2cc([N+](=O)[O-])ccc2nc1Cl
Reaction #6900
2-chloro-3-methyl-6-nitroquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(Nc2nc(Cl)nc3nc[nH]c23)cc1
Reaction #10014
2-Chloro-6-(4-nitro-phenyl-amino)-purine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc([N+](=O)[O-])cc1)c1ccccc1
Reaction #53079
(Z)-3-[1-(4-nitrophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(Br)cc1-c1cc(Nc2ccc([N+](=O)[O-])cc2)nc(N)n1
Reaction #56882
title compound
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=[N+]([O-])c1ccc(N=Nc2ccc(N(CC3CO3)CC3CO3)cc2)cc1
Reaction #65590
4-(N,N-Diglycidylamino)-4'-nitroazobenzene
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccccc1Br
Reaction #65892
2-bromo-N-(4-nitrophenyl)benzamide
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCC(=O)Nc1ccc([N+](=O)[O-])cc1
Reaction #74774
4'-Nitrovaleranilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)Nc1ccc([N+](=O)[O-])cc1
Reaction #80809
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccccc1NC(=O)Nn1c(=O)c(=O)[nH]c2ccccc21
Reaction #82029
N-(N'-(p-nitrophenyl)carboxamidyl)methyl-1,4-dihydroquinoxaline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccccc1NC(=O)Nn1c(=O)c(=O)[nH]c2ccccc21
Reaction #82617
N-(N'-(p-nitrophenyl)carboxamidyl)methyl-1,4-dihydroquinoxaline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=[N+]([O-])c1ccc(Nc2nc3ccccc3[nH]2)cc1
Reaction #169687
N-(4-nitrophenyl)-1H-benzimidazol-2-amine
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=c1[nH]c2cccnc2n1-c1ccc([N+](=O)[O-])cc1
Reaction #169738
3-(4-nitrophenyl)-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
収率 35.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)Cn1c(Nc2ccc([N+](=O)[O-])cc2)nc2cccnc21
Reaction #169863
title compound
収率 101.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CCl)Nc1ccc([N+](=O)[O-])cc1
Reaction #174035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc([N+](=O)[O-])cc1Cl
Reaction #178973
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc2c(c(=O)[nH]1)-c1cc(S(=O)(=O)Nc3ccc([N+](=O)[O-])cc3)ccc1CC2
Reaction #180257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CNc1ccc([N+](=O)[O-])cc1
Reaction #181028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Nc1ccc([N+](=O)[O-])cc1
Reaction #185524
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(C)c(N=Nc2ccc([N+](=O)[O-])cc2)c(C)c2c1OC(C)(C)C2
Reaction #196111
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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