部分構造検索

1118399

CCCCCCCCNCCOc1ccc(SC(C)C)cc1.Cl
Reaction #54288
N-[2-[4-[(1-methylethyl)thio]phenoxy]ethyl]octylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)COC)cc1N=C1SC(=C2Sc3ccc(OCCCl)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #204560
DOI: 10.1039/C8SC04228D
Cc1cc(OC(F)(F)C(Cl)Cl)c([N+](=O)[O-])cc1S(=O)(=O)C=CC#N
Reaction #231640
DOI: 10.1039/C8SC04228D
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCOC(C)=O)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #236002
DOI: 10.1039/C8SC04228D
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCO)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #240517
DOI: 10.1039/C8SC04228D
CC(C)(Oc1ccc(Sc2ccc(Cl)cc2)cc1)C(=O)Cl
Reaction #350252
p-(p-Chlorophenylthio)-phenoxy-isobutyroyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Oc1ccc(Sc2ccc(Cl)cc2)cc1)C(=O)Cl
Reaction #350273
p-(p-Chlorophenylthio)-phenoxy-isobutyroyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Cl)CS(=O)(=O)c1ccc(OC(F)(F)C(Cl)Cl)cc1
Reaction #762504
DOI: 10.1039/C8SC04228D
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCN=[N+]=[N-])cc3N2C)C(=O)N1Cc1ccccc1
Reaction #782468
DOI: 10.1039/C8SC04228D
Cc1cc(OC(F)(F)C(Cl)Cl)c([N+](=O)[O-])cc1S(=O)(=O)C=CC#N
Reaction #926095
title compound
収率 10.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Oc1ccc(Sc2ccc(Cl)cc2)cc1)C(=O)Cl
Reaction #1204367
DOI: 10.1039/C8SC04228D
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCCl)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1216497
DOI: 10.1039/C8SC04228D
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCCl)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329186
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCN(C)C)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329189
title compound
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCO)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329190
title compound
収率 5.3%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(C(C)=O)cc1N=C1SC(=C2Sc3ccc(OCCCl)cc3N2C)C(=O)N1Cc1ccco1
Reaction #1329191
2-(5-acetyl-2-ethylaminophenylimino)-5-[5-(2-chloroethoxy)-3-methyl-3H-benzothiazol-2-ylidene]-3-furan-2-ylmethylthiazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)COC)cc1N=C1SC(=C2Sc3ccc(OCCCl)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329192
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCN=[N+]=[N-])cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329199
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ccc(NC(=O)CN(C)C)cc1N=C1SC(=C2Sc3ccc(OCCOC(C)=O)cc3N2C)C(=O)N1Cc1ccccc1
Reaction #1329211
title compound
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Cl)CS(=O)(=O)c1ccc(OC(F)(F)C(Cl)Cl)cc1
Reaction #2159205
2-Chloro-3-((4-(2,2-dichloro-1,1-difluoroethoxy)phenyl)sulfonyl)propanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ