Substructure Search

NO.Cl

Cl.Nc1nc(C(=NOCF)C(=O)Cl)ns1
Reaction #50757
title compound
Yield 106.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(Cl)cccc2[N+](=O)[O-])CC1
Reaction #61869
4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
Yield 70.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1c([N+](=O)[O-])cnn1-c1c(Cl)cc(C(F)(F)F)c(Cl)c1Cl)C(Cl)Cl
Reaction #63135
5-dichloroacetamido-4-nitro-1-(2,3,6-trichloro-4-trifluoromethyl-phenyl)-pyrazole
Yield 76.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F
Reaction #64580
title compound
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Cl)c(Cl)c1CO
Reaction #69629
compound XX
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Cl)c(Cl)c1CO
Reaction #69632
2,3-dichloro-6-nitrobenzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnccc1CNS(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78006
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C1CCN(Cc2ccccc2)C1)S(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78011
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)Cc2cccnc2)c1.Cl.Cl
Reaction #78013
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])Nc1cc(Cl)nc(Cl)c1
Reaction #85793
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(NC(=O)N(Cc2cccnc2)c2cc(Nc3ccccc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86409
title compound
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(NC(=O)N(Cc2cccnc2)c2cc(Nc3ccccc3N)ncn2)c1Cl
Reaction #86410
title compound
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc(Nc2cc(N(C)C(=O)Nc3c(Cl)c(OC)cc(OC)c3Cl)ncn2)c([N+](=O)[O-])c1
Reaction #86457
title compound
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1cc(F)c(OC)cc1F
Reaction #88267
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1cc(F)c(OC)cc1F
Reaction #88268
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #88269
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(C(F)(F)F)c1
Reaction #88283
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(C(F)(F)F)c1
Reaction #88286
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #88289
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1cc(F)c(F)cc1F
Reaction #88293
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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