p-phenylenediamine

Nc1ccc(Nc2nnc(-c3ccccc3)c3ccccc23)cc1
Reaction #315009
N1-(4-phenylphthalazin-1-yl)benzene-1,4-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C1c2c(Cl)c(Cl)c(Cl)c(Cl)c2C(=O)N1c1ccc(N2C(=O)c3c(Cl)c(Cl)c(Cl)c(Cl)c3C2=O)cc1
Reaction #323570
ivory-yellow material
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=C1c2c(Br)c(Br)c(Br)c(Br)c2C(=O)N1c1ccc(N2C(=O)c3c(Br)c(Br)c(Br)c(Br)c3C2=O)cc1
Reaction #323571
N,N'-(p-phenylene)-bis[3,4,5,6-tetrabromophthalimide]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
Nc1ccc(N)c(N)c1
Reaction #324027
1,2,4-triaminobenzene
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_06
Nc1ccc(NC(=O)Nc2ccc(N)cc2)cc1
Reaction #345982
4,4'-DIAMINO CARBANILID
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
CC(C)(C)OC(=O)Nc1ccc(N)cc1
Reaction #376417
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1oncc1C(=O)Nc1ccc(N)cc1
Reaction #384643
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)cc1
Reaction #386647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(NC(=O)N(c2ccccc2)c2ccccc2)cc1
Reaction #399706
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(NC(=O)c2ccccc2)cc1
Reaction #402650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(NC(=S)Nc2ccc(S(N)(=O)=O)cc2)cc1
Reaction #420309
4-(3-(4-aminophenyl)thioureido)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC1(N)C=CC=C(N)C1
Reaction #459807
m-toluenediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
O=[N+]([O-])[O-].[NH4+]
Reaction #464309
ammonium nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
O=[N+]([O-])[O-].[NH3+]O
Reaction #464312
hydroxylammonium nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
O=[N+]([O-])O
Reaction #464313
nitric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
Oc1cccc2ccccc12
Reaction #465930
1-naphthol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Oc1cccc2ccccc12
Reaction #465931
1-naphthol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Oc1cccc2ccccc12
Reaction #465932
1-naphthol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Oc1cccc2ccccc12
Reaction #465933
1-naphthol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Oc1cccc2ccccc12
Reaction #480295
1-naphthol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
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