4-chlorobiphenyl

COc1cccc(OC)c1-c1ccccc1P(=O)(C1CCCCC1)C1CCCCC1
Reaction #67884
2′-(dicyclohexyl-phosphinoyl)-2,6-dimethoxy-biphenyl
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1ccc(-c2ccccc2)cc1
Reaction #78430
4-chlorobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=C(CC(=O)c1ccc(-c2ccc(Cl)cc2)cc1)C(=O)O
Reaction #198615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=C(CC(=O)c1ccc(-c2ccc(Cl)cc2)cc1)C(=O)O
Reaction #237914
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCOCc1ccc(-c2ccccc2)cc1
Reaction #255273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)COCc1ccc(-c2ccccc2)cc1
Reaction #278451
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C(CC(=O)c1ccc(-c2ccc(Cl)cc2)cc1)C(=O)O
Reaction #377391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OCCc1ccccc1I
Reaction #429917
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
OCCc1ccccc1I
Reaction #430636
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(O)CCC(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #468996
4-(4′-chloro-biphenyl-4-yl)-4-oxo-butyric acid
Ausbeute 13.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Clc1ccc(-c2ccccc2)cc1
Reaction #499991
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=S(=O)(O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #500541
4′-Chlorobiphenyl-4-sulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
c1ccc(-c2ccc(COCC3CC3)cc2)cc1
Reaction #730150
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
OCCOCc1ccc(-c2ccccc2)cc1
Reaction #730151
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(C)COCc1ccc(-c2ccccc2)cc1
Reaction #730155
title compound
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
OCc1ccc(-c2ccccc2)cc1
Reaction #730156
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=S(=O)(O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #738501
4′-chlorobiphenyl-4-sulfonic acid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
O=S(=O)(O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #758008
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=S(=O)(O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #763933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Clc1ccc(-c2ccccc2)cc1
Reaction #794390
4-chlorobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
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