2-bromobenzoic acid

O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccccc1Br
Reaction #5772
2-bromo-N-(4-nitrophenyl)benzamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccccc1Br
Reaction #65892
2-bromo-N-(4-nitrophenyl)benzamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)C[C@H](NC(=O)CNC(=O)c1ccccc1Br)B1O[C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@]2(C)O1
Reaction #70026
2-bromo-N-[2-({(1R)-3-methyl-1-[(3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborol-2-yl]butyl}amino)-2-oxoethyl]benzamide
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(Nc2ccccc2C(=O)O)cnc1Br
Reaction #70324
2-(6-Bromo-5-methylpyridin-3-ylamino)benzoic acid
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccccc1-n1nccn1
Reaction #89437
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccccc1O
Reaction #185455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(Cc1cc2ccccc2n1C)C(=O)c1ccccc1Br
Reaction #201900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCCN(C(=O)c2ccccc2Br)CC1
Reaction #213567
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)c1ccccc1Br
Reaction #221840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C(C)=O)c1ccccc1C(=O)O
Reaction #251407
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1OC(=O)c2ccccc21
Reaction #262884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccccc1Nc1ccc(I)cc1
Reaction #284032
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccccc1Br)N1CC2CN(c3nccc(-c4ccccc4)n3)CC2C1
Reaction #331108
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(c1ccccc1Br)N1CC2CN(c3cnc4ccccc4n3)CC2C1
Reaction #331110
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C1OC2(CCN(Cc3ccccc3)CC2)c2ccccc21
Reaction #338654
1′-benzyl-3H-spiro[isobenzofuran-1,4′-piperidin]-3-one
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)OC(=O)c1ccccc1Br
Reaction #361774
oil
Ausbeute 77710.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
O=C(O)c1ccccc1C(=O)c1ccc2c(c1)OCO2
Reaction #394730
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1cc(S(=O)(=O)Cl)ccc1Br
Reaction #442304
2-Bromo-5-chlorosulfonylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
C[Si](C)(C)c1cccc(Br)c1C(=O)O
Reaction #455736
2-Bromo-6-(trimethylsilyl)benzoic acid
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CN(C)S(=O)(=O)c1ccc(Br)c(C(=O)O)c1
Reaction #459419
2-bromo-5-dimethylaminosulfonylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
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