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758557

CC(C)(c1ccccc1)N1C(=O)c2c(I)cc(Cl)c(Cl)c2C1O
Reaction #49514
3-hydroxy-4,5-dichloro-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)c(Cl)cc(I)c21
Reaction #49515
4,5-dichloro-7-iodoisoindolinone
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
OCC#Cc1ccc(Cl)c(Cl)c1
Reaction #190842
DOI: 10.1039/C8SC04228D
CCOC(=O)C#Cc1ccc(Cl)c(Cl)c1
Reaction #253976
DOI: 10.1039/C8SC04228D
O=C1C(=O)N(C/C=C/c2ccc(Cl)c(Cl)c2)c2ccccc21
Reaction #339798
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=O)N(CC#Cc2ccc(Cl)c(Cl)c2)c2ccccc21
Reaction #339801
1-[3-(3,4-dichlorophenyl)prop-2-yn-1-yl]-1H-indole-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(Cc2cc(I)cc(Cl)c2Cl)c1=O
Reaction #362032
3-(2,3-dichloro-5-iodophenylmethyl)-1-methyl-6-trifluoromethyluracil
Ausbeute 110.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(I)ccc(Cl)c1Cl
Reaction #409176
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1c(I)ccc(Cl)c1Cl
Reaction #409177
2,3-Dichloro-6-iodobenzoic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(-c2ccc(Cl)c(Cl)c2)cc1)[C@H](O)CCc1cccnc1.O=C(O)C(=O)O
Reaction #467178
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CSCCN1c1ccc(Cl)c(Cl)c1
Reaction #499169
light brown oil
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(Cl)c(Cl)cc1N
Reaction #675964
desired product
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1
OCCOc1ccnc(Oc2cc(Cl)c(Cl)cc2I)c1
Reaction #675972
desired product
Ausbeute 33.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCOc1ccnc(Oc2cc(Cl)c(Cl)cc2I)c1
Reaction #675973
desired product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCOc1ccnc(Oc2cc(Cl)c(Cl)cc2I)c1
Reaction #675974
desired product
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)NCCOc1ccnc(Oc2cc(Cl)c(Cl)cc2I)c1
Reaction #675975
desired product
Ausbeute 155.3%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(-c2cc(Cl)c(Cl)cc2I)c1
Reaction #675983
desired product
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCCCCCC#Cc1ccc(Cl)c(Cl)c1
Reaction #897881
DOI: 10.1039/C8SC04228D
O=C1CSCCN1c1ccc(Cl)c(Cl)c1
Reaction #930787
light brown oil
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(Cl)c(Cl)c2)cc1[N+](=O)[O-]
Reaction #946458
solid
DOI: 10.6084/m9.figshare.5104873.v1
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