Substructure Search

CN1CCN(c2ccc(N)c(N)c2)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+](=O)[O-])c(N)c2)CC1
Reaction #41798
5-(4-Methyl-piperazin-1-yl)-2-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
Yield 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
Cc1cc(C)nc(N2CCN(c3ccc([N+](=O)[O-])c(Cl)c3)CC2)c1
Reaction #66144
1-(3-chloro-4-nitro-phenyl)-4-(4,6-dimethyl-pyridin-2-yl)-piperazine
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])c2)CC1
Reaction #86412
title compound
Yield 55.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86413
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(Nc3cc(NC)ncn3)c([N+](=O)[O-])c2)CC1
Reaction #86414
title compound
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(Nc3cc(N(C)C(=O)Nc4c(Cl)c(OC)cc(OC)c4Cl)ncn3)c([N+](=O)[O-])c2)CC1
Reaction #86415
title compound
Yield 22.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(Nc3cc(N(C)C(=O)Nc4c(Cl)c(OC)cc(OC)c4Cl)ncn3)c(N)c2)CC1
Reaction #86416
title compound
Yield 89.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(CC)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86417
title compound
Yield 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc([N+](=O)[O-])c(N)c2)CC1
Reaction #86445
title compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(C(C)C)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1.O=P(O)(O)O
Reaction #86468
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #86469
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])c2)CC1
Reaction #86471
title compound
Yield 70.5%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next