Teilstruktursuche

C1=CSC(=C1)Cl

CC(C)(C)OC(=O)N1CCN(c2cccs2)CC1
Reaction #398
Ausbeute 0.0%
Br.Br.O=C(C[C@@H]1NCCC[C@H]1O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #4366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.Br.O=C(C[C@@H]1NCCC[C@H]1O)Cn1cnc2cc(Cl)sc2c1=O
Reaction #4368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2c(Br)c(Cl)sc2c1=O
Reaction #4369
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2c(Br)c(Cl)sc12
Reaction #4375
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2ccccc2c1)c1ccsc1Cl
Reaction #62288
title compound
Ausbeute 52.1%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2cc(-c3n[nH]c4sccc34)ccc2c1
Reaction #62289
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc(Cl)s1
Reaction #65609
2-benzoyl-5-chlorothiophene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc(C(=O)C2(Cl)CC=CS2)c1)C1(Cl)CC=CS1
Reaction #65610
1,3-Bis(2-chlorothiophenoyl)Benzene
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NS(=O)(=O)c1ccc(Cl)s1)c1ccc([N+](=O)[O-])cc1
Reaction #66418
titled compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=O)NS(=O)(=O)c2ccc(Cl)s2)ccc1N
Reaction #66427
N-(4-amino-3-methylphenyl){[(5-chloro(2-thienyl))sulfonyl]amino}-carboxamide
Ausbeute 136.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1sc(Cl)cc1F
Reaction #66446
desire product
Ausbeute 108.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(-n2c(=O)[nH]c3ccccc3c2=O)cc1)NS(=O)(=O)c1sc(Cl)cc1F
Reaction #66447
desired product
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(C)cc(C)nc2n1-c1ccc(CCNC(=O)NS(=O)(=O)c2ccc(Cl)s2)cc1
Reaction #78708
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)c1ccc(Cl)s1
Reaction #94756
4-(5-chloro-2-thienyl)-4-ketobutyric acid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)c1ccc(Cl)s1
Reaction #94779
4-(5-chloro-2-thienyl)-4-ketobutyric acid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)c1ccc(Cl)s1
Reaction #94802
4-(5-chloro-2-thienyl)-4-ketobutyric acid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(F)c(F)c1Nc1ccc(I)cc1F)c1ccc(Cl)s1
Reaction #160592
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCC(=O)c1ccc(Cl)s1
Reaction #172985
DOI: 10.1039/C8SC04228D
Cc1cc(COc2ncc(Cl)nc2NS(=O)(=O)c2ccc(Cl)s2)no1
Reaction #173194
DOI: 10.1039/C8SC04228D
Seite 1Weiter