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CN1CCN(c2ccc(N)c(N)c2F)CC1

CN1CCN(c2ccc([N+](=O)[O-])c(N)c2F)CC1
Reaction #41797
2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41802
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41803
2
Выход 94.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41804
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41805
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41806
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41807
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41809
diamine
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2c(Cl)cc([N+](=O)[O-])c(N)c2F)CC1
Reaction #199729
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #224535
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #287662
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #399891
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc([N+](=O)[O-])c(N)c2F)CC1
Reaction #781660
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #1044007
DOI: 10.1039/C8SC04228D
CN1CCN(c2c(F)cc(N)c(N)c2F)CC1
Reaction #1091772
4,6-difluoro-5-(4-methylpiperazin-1-yl)-1, 2-phenylenediamine
Выход 100.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(Cl)c(N2CCN(CCO)CC2)c1F
Reaction #1151547
title compound
Выход 67.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #1323903
DOI: 10.1039/C8SC04228D
CCN1CCN(c2c(Cl)cc([N+](=O)[O-])c(N)c2F)CC1
Reaction #1332619
title compounds
Выход 63.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc([N+](=O)[O-])c(N)c2F)CC1
Reaction #2002878
2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #2002883
2
DOI: 10.6084/m9.figshare.5104873.v1
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