4-bromo-2-fluorobenzaldehyde

CC(C)(C)OC(=O)Nc1ccc(C=O)c(F)c1
Reaction #315
Ausbeute 83.6%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)Nc1ccc(C=O)c(F)c1
Reaction #316
Ausbeute 97.5%750 AstraZeneca ELN dataset
COC(=O)c1cc2ccc(Br)cc2s1
Reaction #43709
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1cc(Br)ccc1C1OCCO1
Reaction #53587
2-(2-fluoro-4-bromophenyl)dioxolan
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)Cc1ccc(-c2[nH]c3cccc4c3c2CCNC4=O)cc1F
Reaction #61605
2-(4-dimethylaminomethyl-3-fluoro-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)[S@@](=O)/N=C/c1ccc(Br)cc1F
Reaction #85696
(R,E)-N-(4-bromo-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Fc1cc(Br)ccc1C1OCCO1
Reaction #165409
title compound
Ausbeute 102.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccncc1N1CCN(c2ccc(C=O)c(F)c2)C1=O
Reaction #167335
2-Fluoro-4-[3-(4-methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzaldehyde
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1cc(Br)ccc1C1OCCO1
Reaction #182339
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc(-c2ccc(F)cc2)cc1F
Reaction #187363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(c1ccc(Br)cc1F)c1ccccc1C(F)(F)F
Reaction #206726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(C#N)Cc1ccc(Br)cc1F
Reaction #232172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O)c1ccc(Br)cc1F
Reaction #271320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Fc1cc(Br)ccc1C1OCCO1
Reaction #296680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Fc1cc(Br)ccc1C1OCCO1
Reaction #316379
88
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)N=Cc1ccc(Br)cc1F
Reaction #324427
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)N=Cc1ccc(Br)cc1F
Reaction #324468
title compound
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #326815
liquid
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #326816
liquid
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCOC(=O)c1cc2ccc(Br)cc2s1
Reaction #337446
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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