2-nitrotoluene

O=C(O)c1ccccc1[N+](=O)[O-]
Reaction #9848
2-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77928
4-(2-nitrophenyl)-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77929
4-(2-nitrophenyl)-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77930
4-(2-nitrophenyl)-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77931
4-(2-nitrophenyl)-butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C([O-])CCCc1ccccc1[N+](=O)[O-]
Reaction #77932
4-(2-nitrophenyl)butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77933
4-(2-nitro-phenyl)butyronitrile
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#CCCCc1ccccc1[N+](=O)[O-]
Reaction #77938
4-(2-nitrophenyl)butyronitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccccc1[N+](=O)[O-]
Reaction #176344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccccc1[N+](=O)[O-]
Reaction #181009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1[N+](=O)[O-]
Reaction #183604
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1[N+](=O)[O-]
Reaction #215041
nitrotoluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Cc1ccccc1[N+](=O)[O-]
Reaction #245289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1[N+](=O)[O-]
Reaction #256074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cccc([N+](=O)[O-])c1[N+](=O)[O-]
Reaction #258431
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccccc1[N+](=O)[O-]
Reaction #265121
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccc([N+](=O)[O-])c1[N+](=O)[O-]
Reaction #297082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccccc1CN1CCCC1
Reaction #326381
liquid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cccc([N+](=O)[O-])c1[N+](=O)[O-]
Reaction #346272
dinitrotoluene
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=[N+]([O-])c1ccccc1CBr
Reaction #348483
o-nitrobenzyl bromide
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_08
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