3,5-dibromo-2-hydroxybenzaldehyde

O=C1NC(=O)C(=Cc2cc(Br)cc(Br)c2O)C(=O)N1
Reaction #84047
product 1a
Rendimiento 84.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=c1cc(N2CCN(Cc3cc(Br)cc(Br)c3O)CC2)nc[nH]1
Reaction #178445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1ccc2cc(Br)cc(Br)c2o1
Reaction #652974
6,8-dibromocoumarin
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC(C)(C)NCc1cc(Br)cc(Br)c1O.Cl
Reaction #703592
N-tert.butyl-3,5-dibromo-2-hydroxy-benzylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_02
CC(C)(C)[N+]([O-])=Cc1cc(Br)cc(Br)c1O
Reaction #762664
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=c1ccc2cc(Br)cc(Br)c2o1
Reaction #929050
6,8-dibromocoumarin
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=c1ccc2cc(Br)cc(Br)c2o1
Reaction #936650
6,8-dibromocoumarin
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
COc1ccc(-c2cc3cc(Br)cc(Br)c3oc2=O)cc1
Reaction #1011002
6,8-Dibromo-3-(4-methoxy-phenyl)-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=Cc1cc(-c2ccc(Cl)c(Cl)c2)cc(-c2ccc(Cl)c(Cl)c2)c1O
Reaction #1016773
3,3″,4,4″-Tetrachloro-4′-hydroxy-[1,1′:3′,1″-terphenyl]-5′-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=Cc1cc(-c2ccc(C(F)(F)F)c(Cl)c2)cc(-c2ccc(C(F)(F)F)c(Cl)c2)c1O
Reaction #1016775
3,3″-Dichloro-4′-hydroxy-4,4″-bis(trifluoromethyl)-[1,1′:3′,1″-terphenyl]-5′-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC(C)[C@H](N=Cc1cc(Br)cc(Br)c1O)C(=O)O
Reaction #1120075
N-(3,5-dibromosalicylidene)-(S)-valine
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_05
O=C(O)c1ccc(NC(=S)NN=Cc2cc(Br)cc(Br)c2O)cc1
Reaction #1381908
title compound
Rendimiento 42.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
OCc1cc(Br)cc(Br)c1O
Reaction #1487970
2-hydroxy-3,5-dibromobenzenemethanol
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)(C)[N+]([O-])=Cc1cc(Br)cc(Br)c1O
Reaction #1618422
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_03
O=Cc1cc(-c2ccc(Cl)c(Cl)c2)cc(-c2ccc(Cl)c(Cl)c2)c1O
Reaction #1941389
3,3″,4,4″-Tetrachloro-4′-hydroxy-[1,1′:3′,1″-terphenyl]-5′-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
O=Cc1cc(-c2ccc(C(F)(F)F)c(Cl)c2)cc(-c2ccc(C(F)(F)F)c(Cl)c2)c1O
Reaction #1941391
3,3″-Dichloro-4′-hydroxy-4,4″-bis(trifluoromethyl)-[1,1′:3′,1″-terphenyl]-5′-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CC1(C)CCC2=C(C1=O)C(c1cc(Br)cc(Br)c1O)n1nccc1N2
Reaction #1949564
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
O=c1ccc2cc(Br)cc(Br)c2o1
Reaction #1958248
6,8-dibromocoumarin
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_08
O=c1cc(N2CCN(Cc3cc(Br)cc(Br)c3O)CC2)nc[nH]1
Reaction #2080634
6-[4-(3,5-Dibromo-2-hydroxy-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_01
O=C(O)c1ccc(NC(=S)NN=Cc2cc(Br)cc(Br)c2O)cc1
Reaction #2213331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)