部分構造検索

Cl.Cl.NC1CN2CCC1CC2

COc1ccc(C(=O)NC2CN3CCC2CC3)c(OC)c1.Cl
Reaction #3857
white solid
収率 23.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccccc1C(=O)NC1CN2CCC1CC2.Cl
Reaction #3858
N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(OC)c(C(=O)[NH+]([O-])C2CN3CCC2CC3)cc1Cl.Cl
Reaction #3859
N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1N(c2cccc(Cl)c2)CCN1C1CN2CCC1CC2
Reaction #5047
1-(1-azabicyclo[2.2.2]oct-3-yl)-3-(3-chlorophenyl)-imidazolidin-2-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(CCl)NC1CN2CCC1CC2
Reaction #5597
solid
収率 144.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(SCC(=O)NC2CN3CCC2CC3)cc(C(C)(C)C)c1O.Cl
Reaction #5598
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)ccc2c1C1CCCCC1O2
Reaction #5980
1-amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(Br)ccc2s1
Reaction #43728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NC1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2s1
Reaction #43730
hydrochloride
収率 48.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc2sc(C(=O)NC3CN4CCC3CC4)cc2c1
Reaction #43731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(Cl)cc(Cl)c2o1
Reaction #43732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)cc2cc(C(=O)N[C@H]3CN4CCC3CC4)oc12.Cl.Cl
Reaction #43733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2o1
Reaction #43734
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CN2CCC1CC2)c1cc2cc([N+](=O)[O-])ccc2o1
Reaction #43735
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2ccc([N+](=O)[O-])cc2o1
Reaction #43738
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cccc([N+](=O)[O-])c2o1
Reaction #43740
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(F)cc(F)c2o1
Reaction #43742
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(F)cc(Br)c2o1
Reaction #43743
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1sc2cc(F)ccc2c1Cl
Reaction #43746
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@@H]1CN2CCC1CC2)c1sc2cc(F)ccc2c1Cl
Reaction #43747
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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