Busqueda de Subestructura

7035

Nc1cc(Cl)ccc1[N+](=O)[O-]
Reaction #4067
2-nitro-5-chloroaniline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])c(N)cc1Cl
Reaction #51630
5-Chloro-4-methoxy-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(N)cc1Cl.Cl.Cl
Reaction #51631
4-Chloro-5-methoxy-benzene-1,2-diamine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Cl)cc1N1CCCCC1
Reaction #61164
title compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61165
title compound
Rendimiento 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-n2ccnc2)cc1N1CCCCC1
Reaction #61168
title compound
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61177
title compound
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc(N)c1[N+](=O)[O-]
Reaction #72779
desired product
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc(N)c1[N+](=O)[O-]
Reaction #72780
desired product
Rendimiento 46.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75127
31.7
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75128
31.5
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F)C(F)(F)F
Reaction #82074
solid
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F
Reaction #82075
crystalline yellow solid
Rendimiento 6.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F)C(F)(F)F
Reaction #82662
solid
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(F)c(Cl)c1F
Reaction #82663
crystalline yellow solid
Rendimiento 6.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Cl)cc1-n1nnc2ncccc21
Reaction #163171
4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamine
Rendimiento 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cnnn1-c1cc(Cl)ccc1[N+](=O)[O-]
Reaction #163185
1-(5-chloro-2-nitro-phenyl)-5-isopropyl-1H-[1,2,3]triazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc(N)c1[N+](=O)[O-]
Reaction #172319
methyl 3-amino-5-chloro-2-nitrobenzoate
Rendimiento 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cc(Cl)c(C#Cc2ccccc2)cc1[N+](=O)[O-]
Reaction #173343
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc([N+](=O)[O-])c(N3CCCC(F)C3)c2)CC1
Reaction #173604
DOI: 10.1039/C8SC04228D
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