4-bromophenylacetic acid

CCOC(=O)Cc1ccc(Br)cc1
Reaction #1303
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Cc1ccc(Br)cc1
Reaction #1458
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Cc2ccc(Br)cc2)n3C)ccn1
Reaction #41767
(4-{2-[(4-bromophenyl)methyl]-1-methylbenzimidazol-5-yloxy)-(2-pyridyl))-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(NC(=O)Cc1ccc(Br)cc1)C(=O)OCC(C)C
Reaction #51363
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)Cc1ccc(Br)cc1
Reaction #52839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCCCNC(=O)Cc1ccc(Br)cc1
Reaction #76093
2-(4-bromo-phenyl)-N-heptyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(Cc1ccc(Br)cc1)Nc1ccccc1
Reaction #79900
N1-phenyl-2-(4-bromophenyl)acetamide
収率 68.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)Cc1ccc(Br)cc1
Reaction #81582
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)Cc1ccc(Br)cc1
Reaction #81646
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)Cc1ccc(Br)cc1
Reaction #83573
4-bromophenylacetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)Cc1ccc(Br)cc1
Reaction #186146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)Cc1ccc(Br)cc1
Reaction #193067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1ccc(Br)cc1
Reaction #204461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1ccc(Br)cc1
Reaction #204687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C1CCCCN1C(=O)Cc1ccc(Br)cc1)N(C)C
Reaction #213092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)Cc1ccc(Br)cc1
Reaction #215693
4-bromo-phenylacetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCC(NC(=O)Cc1ccc(Br)cc1)C(=O)OCC(C)C
Reaction #220552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(Cc1ccc(Br)cc1)Nc1ccccc1
Reaction #220602
2-(4-Bromophenyl)-N-phenyl-acetamide
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(Cc1ccc(Br)cc1)NCc1ccccc1
Reaction #220603
N-Benzyl-2-(4-bromo-phenyl)-acetamide
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)NC(=O)Cc1ccc(Br)cc1
Reaction #225929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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