4-anilinophenol

C/C=C/C(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #54322
4-Anilinophenyl crotonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #54323
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(O)/C=C\C(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #54324
4-Anilinophenyl hydrogen maleate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COC(=O)CCCOc1ccc(Nc2ccccc2)cc1
Reaction #250116
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)C=CC(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #292888
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1oc(-c2ccccc2)nc1CCOc1ccc(Nc2ccccc2)cc1
Reaction #439626
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
O=C(CCCc1ccc([N+](=O)[O-])cc1)Oc1ccc(Nc2ccccc2)cc1
Reaction #480696
4-anilinophenyl 4-(4-nitrophenyl)butanoate
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CC(C)(C)[Si](C)(C)Oc1ccc(Nc2ccccc2)cc1
Reaction #603076
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
c1ccc(COc2ccc(Nc3ccccc3)cc2)cc1
Reaction #603077
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)(C)[Si](C)(C)Oc1ccc(Nc2ccccc2)cc1
Reaction #606108
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)(C)OC(=O)N1CCC[C@@H]1COc1ccc(Nc2ccccc2)cc1
Reaction #837161
title product
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
CC=CC(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #1217855
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
C/C=C/C(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #1693595
4-Anilinophenyl crotonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_04
—
Reaction #1693596
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_04
O=C(O)/C=C\C(=O)Oc1ccc(Nc2ccccc2)cc1
Reaction #1693597
4-Anilinophenyl hydrogen maleate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_04
CC(C)(C)OC(=O)N1CCC[C@@H]1COc1ccc(Nc2ccccc2)cc1
Reaction #1996848
title product
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_12
COC(=O)CCCOc1ccc(Nc2ccccc2)cc1
Reaction #2250790
methyl 4-(p-anilinophenoxy)butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_01
CC(C)(C)[Si](C)(C)Oc1ccc(Nc2ccccc2)cc1
Reaction #2360056
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
O=C(C=Cc1ccccc1)Oc1ccc(Nc2ccccc2)cc1
Reaction #2401835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
Oc1ccc(Nc2ccccc2)cc1
Reaction #2441219
N-(4-hydroxyphenyl)aniline
Ausbeute 27.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07