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Nc1cc(Cl)cc(Cl)c1

O=c1[nH]c2cc(Cl)cc(Cl)c2c(=O)o1
Reaction #3199
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(NC(=O)OC(C)(C)C)cc(Cl)c(OC)c1Cl
Reaction #3222
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)cc(Cl)c(OC)c1Cl
Reaction #3223
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Cl)cc(Cl)c1)c1ccccc1SSc1ccccc1C(=O)Nc1cc(Cl)cc(Cl)c1
Reaction #3814
title compound
Ausbeute 22.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #51302
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #51318
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #51321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3ccccc3[nH]2)cc1NC(=S)Nc1cc(Cl)cc(Cl)c1
Reaction #53767
1-(3,5-Dichloro-phenyl)-3-[5-(1H-indol-2-yl)-2-methoxy-phenyl]-thiourea
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NC(=S)Nc1cc(Cl)cc(Cl)c1
Reaction #53770
1-(3,5-Dichloro-phenyl)-3-[5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-thiourea
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54029
title compound
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
Reaction #54208
pentachloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1cc(Cl)cc(Cl)c1
Reaction #55534
methyl N-(3,5-dichlorophenyl)-carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(Oc2ccc(Cl)c3ccccc23)c(Cl)c1
Reaction #65602
4-(4-chloro-1-naphthoxy)-3,5-dichloroaniline
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)cc(N=Cc2ccccc2)c1
Reaction #75371
N-benzylidene-3,5-dichloroaniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #75639
Compound 1
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2cccc(F)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75644
Compound 8
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc3ccccc3c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75645
Compound 11
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2c3ccccc3CCC12
Reaction #75646
Compound 12
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75647
Compound 14
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccccc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75648
Compound 15
DOI: 10.6084/m9.figshare.5104873.v1
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