DNFB

CC(=O)NCCn1nnnc1Sc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #74876
1-(2-acetamidoethyl)-5-(2,4-dinitrophenylthio)tetrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=[N+]([O-])c1ccc(NCCO)c([N+](=O)[O-])c1
Reaction #76418
N-(2,4-dinitrophenyl)ethanolamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=[N+]([O-])c1ccc(Nc2cccc(C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)c2)c([N+](=O)[O-])c1
Reaction #78795
N-[3-(perfluorooctyl)phenyl]-2,4-dinitrobenzenamine
Yield 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)CCNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #82439
solid
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1cc([N+](=O)[O-])ccc1F
Reaction #182038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(Nc2cccc(C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)c2)c([N+](=O)[O-])c1
Reaction #183410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)NCCn1nnnc1Sc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #206956
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(c1ccc([N+](=O)[O-])cc1[N+](=O)[O-])(C(F)(F)F)C(F)(F)F
Reaction #208456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #225302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCN(OC1C(O)C(COC(c2ccccc2)(c2ccccc2)c2cccc(OC)c2OC)OC1n1ccc(=O)[nH]c1=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #267716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1cn(-c2ccc([N+](=O)[O-])cc2[N+](=O)[O-])c(C)n1
Reaction #334955
Ethyl 1-(2,4-dinitrophenyl)-2-methylimidazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCOC(=O)CSc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #362623
red-brown solid
Yield 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COC(=O)CC(Nc1ccc([N+](=O)[O-])cc1[N+](=O)[O-])c1ccc(-c2ccccc2)cc1
Reaction #372223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1cc([N+](=O)[O-])ccc1F
Reaction #381390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1ccccc1Nc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #393008
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1cc([N+](=O)[O-])ccc1F
Reaction #396719
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc(Sc2ccccc2)c([N+](=O)[O-])c1
Reaction #417096
2,4-dinitrophenyl phenyl sulfide
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CCCCCCN(O[C@@H]1[C@H](O)[C@@H](COC(c2ccccc2)(c2ccccc2)c2cccc(OC)c2OC)O[C@H]1n1ccc(=O)[nH]c1=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #440790
5′-O-(dimethoxytrityl)-2′-O-[hexyl-N-(2,4-dinitrophenyl)amino]uridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1ccccc1NC(=O)c1ccc(Oc2ccc([N+](=O)[O-])cc2[N+](=O)[O-])cc1
Reaction #480677
4-(2,4-dinitrophenoxy)-2′-methybenzanilide
Yield 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CCCCN1CC2CN(c3ccc([N+](=O)[O-])cc3[N+](=O)[O-])CC(C1)C2(C)C
Reaction #481679
7-(n-butyl)-3-(2,4-dinitrophenyl)-9,9-dimethyl-3,7-diazabicyclo-[3.3.1]nonane
Yield 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
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