azanium

Nc1cc(Cl)ccc1[N+](=O)[O-]
Reaction #4067
2-nitro-5-chloroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1ccc(C2c3c(C)c(N)c(C)c(C)c3OC2(C)C)cc1
Reaction #57400
title compound
Yield 87.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)[C@@H](c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #57401
title compound
Yield 75.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(N)ccc1-c1cnnc(C)c1
Reaction #87402
title compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(C(=N)NS(=O)(=O)C=Cc2ccc(Cl)c(Cl)c2)cc1OC
Reaction #94484
N-(3,4-DICHLOROSTYRYLSULFONYL)-3,4-DIMETHOXYBENZAMIDINE
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
NC(=O)c1cc(Cl)c[nH]1
Reaction #160862
above compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(c1ccc(NC=O)c([N+](=O)[O-])c1)n1ccnc1
Reaction #172970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)nc(NCCO)nc1OCCOc1ncc(Br)cn1
Reaction #172980
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1nc(CC)c(N)c1C(N)=O
Reaction #173066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])CCc1ccc(Oc2ccccc2F)nc1
Reaction #173198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C1CCCN1c1cc2c(cn1)-c1nc(-c3ncnn3-c3ccc(F)cc3F)cn1CCO2
Reaction #173203
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC1(OC)CC(c2cc(NC(=O)C(C)(C)c3ccccn3)n(C(C)(C)C)n2)C1
Reaction #173244
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)Oc1cccc2ccc(-c3ccccn3)nc12
Reaction #173279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(COCCCNC2CC2)cc1
Reaction #173403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1c(F)c(NCCCc2ccccn2)c2c3c1c(=O)c(C(=O)O)cn3C1(CCOC1)CO2
Reaction #173406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(C(=O)CCCCOCc2ccccc2)cc1
Reaction #173439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc([N+](=O)[O-])cn1
Reaction #173473
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC(O)c1ccc(C2=CCCC2CCCc2ccc(C(=O)O)s2)cc1
Reaction #173505
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCC1CNCC1c1ccccc1
Reaction #173586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nc(OCCO)c(-c2ccc3c(c2)OCO3)c1N
Reaction #173640
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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