Substructure Search

Oc1ccccc1Br

CCOC(=O)c1cnc2cc(OCC)c(N3CCN(C(C)C)CC3)cc2c1Nc1ccc(F)cc1F
Reaction #97
Yield 65.4%
O=[N+]([O-])c1ccc(OCc2cccc(F)c2)c(Br)c1
Reaction #6912
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(OCc2ccccc2)c(Br)c1
Reaction #44353
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(C=Cc2ccccc2)c(C)c(C#N)c1NC(=O)C(C)(C)C
Reaction #45549
N-(3-Bromo-6-cyano-2-methoxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(NC(=O)C(C)(C)C)c(O)c(Br)c1C=Cc1ccccc1
Reaction #45552
compound
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(-c2ccccc2)c(C)c(C#N)c1NC(=O)C(F)(F)F
Reaction #45573
compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C#N)c(C)c(-c2ccccc2)c1Br
Reaction #45575
compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCOCC4)[nH]c3cc2Br)CC1
Reaction #48164
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCOCC4)n(-c4ccnc(Cl)c4)c3cc2Br)CC1
Reaction #48165
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCC(F)(F)CC4)[nH]c3cc2Br)CC1
Reaction #48166
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCC(F)(F)CC4)n(-c4ccnc(Cl)c4)c3cc2Br)CC1
Reaction #48167
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc(-c2ccc(C(F)(F)F)cc2)nc1-c1ccc(-c2cc(Br)c(OCC(=O)O)c(Br)c2)cc1
Reaction #75937
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1)Oc1c(Br)cc(-c2ccc(-c3nc(-c4ccc(C(F)(F)F)cc4)oc3C)cc2)cc1Br
Reaction #75938
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(O)c(Br)cc1F
Reaction #76771
2-bromo-4-fluoro-5-nitrophenol
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc([N+](=O)[O-])c(F)cc1Br
Reaction #76772
2-bromo-4-fluoro-5-nitrophenyl isopropyl ether
Yield 85.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc(C(=O)C(OC)c3ccc(N4CCOCC4)cc3)n2)cc(OC)c1Br
Reaction #84772
1-(4-(4-bromo-3,5-dimethoxyphenyl)oxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)-ethanone
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc(C(=O)C(OC)c3ccc(-n4cccn4)cc3)n2)cc(OC)c1Br
Reaction #84777
2-(4-(1H-pyrazol-1-yl)phenyl)-1-(4-(4-bromo-3,5-dimethoxyphenyl)thiazol-2-yl)-2-methoxyethanone
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nnc(-c2ccc(C(OC)C(=O)c3ccc(-c4cc(OC)c(Br)c(OC)c4)o3)cc2)o1
Reaction #84800
1-(5-(4-bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-(4-(5-ethyl-1,3,4-oxadiazol-2-yl)phenyl)-2-methoxyethanone
Yield 12.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(C(=O)C(OC)c3cccc4ncccc34)o2)cc(OC)c1Br
Reaction #84808
1-(5-(4-bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-methoxy-2-(quinolin-5-yl)ethanone
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(C(=O)C(OC)c3ccc4c(c3)nnn4C)o2)cc(OC)c1Br
Reaction #84819
1-(5-(4-bromo-3,5-dimethoxyphenyl)furan-2-yl)-2-methoxy-2-(1-methyl-1H-benzo[d][1,2,3]triazol-5-yl)ethanone
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
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