4-Butylbenzoic acid

CCCCc1ccc(C(=O)NC2CN3CCC2CC3)cc1
Reaction #290067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCc1ccc(C(=O)Nc2nc3cccc(-c4ccoc4)n3n2)cc1
Reaction #290087
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCc1ccc(C(=O)NC(Cc2ccc(C(F)(F)F)cc2)C(O)c2ccc(F)cc2)cc1
Reaction #780623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCc1ccc(C(=O)Cl)cc1
Reaction #982057
p-n-butyl benzoylchloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_08
CCCCc1ccc(C(=O)Cl)cc1
Reaction #1220448
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCCCc1ccc(C(=O)Nc2ccc3oc(N(C)C4CCN(C)CC4)nc3c2)cc1
Reaction #1262119
desired product
المردود 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CCCCCCC(C)CCCOc1ccc(OC(=O)c2ccc(CCCC)cc2)cc1
Reaction #1694956
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_09
CCCCc1ccc(C(=O)NC(Cc2ccc(C(F)(F)F)cc2)C(O)c2ccc(F)cc2)cc1
Reaction #1697406
title compound
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
CCCC[C@H]1CC[C@@H](C(=O)O)CC1
Reaction #1796331
cis-4- n-butylcyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_08
CCCCc1ccc(C(=O)N[C@H](CCCNC(N)=N[N+](=O)[O-])C(=O)NCc2ccc(CNC(N)=O)cc2)cc1
Reaction #2040203
(R)-N-[[4-(Aminocarbonylaminomethyl)phenyl]methyl]-N5 -[amino(nitroimino)methyl]-N2 -(4-butylbenzoyl)-ornithinamide
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_09
CCCCc1ccc(C(=O)N[C@@H]2CN3CCC2CC3)cc1
Reaction #2175494
(S)-4-butyl-N-(quinuclidin-3-yl)benzamide
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCCCc1ccc(C(=O)Nc2nc3cccc(-c4ccoc4)n3n2)cc1
Reaction #2470019
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09