Teilstruktursuche

CC(C)C(=S)N

CN(C)c1ccccc1CSC1=NC(C)(C)C(SCc2ccccc2N(C)C)=N1
Reaction #3340
2,4-bis(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #3341
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #3342
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cccc(CSC2=NC(C)(C)C(SCc3cccc(N(C)C)c3)=N2)c1
Reaction #3343
2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)N=C(SCc2cccc3cccnc23)N=C1SCc1cccc2cccnc12
Reaction #3344
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cccc(CSC2=NC(C)(C)C(SCc3cccc(N(C)C)c3)=N2)c1
Reaction #3345
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(CSC2=NC(C)(C)C(SCc3ccc(N(C)C)cc3)=N2)cc1
Reaction #3346
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)NC(SCc2ccccc2)=NC1=S
Reaction #3347
2-benzylthio-5,5-dimethylimidazolin-4-thione
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(C2CCCCC2)n1
Reaction #4496
ethyl 2-cyclohexyl-4-thiazoleacetate
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C(C)(C#N)c1ccc(Cl)cc1
Reaction #6036
N-methyl-2-(4-chlorophenyl)-2-cyano-thiopropionamide
Ausbeute 31.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C(C)(C#N)c1ccc(-n2ccnc2)cc1
Reaction #6038
N-methyl-2-[4-(1-imidazolyl)-phenyl]-2cyanothiopropionamide
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(Cc2ccccc2)C(=S)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #9418
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #9426
product
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(C(N)=O)C(=S)Nc1cccc(Oc2ccccc2)c1
Reaction #62035
2-cyano-2-(3-phenoxy-phenylthiocarbamoyl)-acetamide
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(C(N)=O)C(=S)Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62039
crude product
Ausbeute 82.5%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(O)nsc1Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62040
5-[4-(2,5-Dichloro-phenoxy)-3-fluoro-phenylamino]-3-hydroxy-isothiazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)C(N)=S
Reaction #66959
title compound
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CCl)cs1.Cl
Reaction #80967
crude desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(C(C)C)n1
Reaction #80972
desired compound
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(C(C)C)s1
Reaction #80996
desired compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter