(4-hydroxyphenyl)-phenylmethanone

O=C(Cl)c1ccc(C(=O)c2ccccc2)cc1
Reaction #6549
4-chloroformylbenzophenone
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=COc1ccc(C(=O)c2ccccc2)cc1
Reaction #9797
4-vinyloxybenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(O)(COc1ccc(C(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64157
title compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C=CC(=O)OCCCCOCC(O)COc1ccc(C(=O)c2ccccc2)cc1
Reaction #69389
yellow oil
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(=O)OCCCCOCC(O)COc1ccc(C(=O)c2ccccc2)cc1
Reaction #71012
yellow oil
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C(C)C(=O)Oc1ccc(C(=O)c2ccccc2)cc1
Reaction #73689
compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1ccccc1)c1ccc(OCc2ccccc2)cc1
Reaction #157917
(4-Benzyloxy-phenyl)-phenyl-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1ccccc1)c1ccc(OC(=O)C2CCCCC2)cc1
Reaction #183851
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccccc1)c1ccc(OCCc2c[nH]cn2)cc1
Reaction #234831
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Oc1ccc(C(=O)c2ccccc2)cc1
Reaction #268363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Oc1ccc(C(=C(CCCl)c2ccccc2)c2ccccc2)cc1
Reaction #269263
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCOc1ccc(C(=O)c2ccccc2)cc1
Reaction #293227
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=CC(=O)Oc1ccc(C(=O)c2ccccc2)cc1
Reaction #318646
oily product
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
Cl.O=C(c1ccccc1)c1ccccc1
Reaction #336455
benzophenone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
O=C(c1ccccc1)c1ccc(OCCCCCBr)cc1
Reaction #336456
4-[(5-bromopentyl)oxy]benzophenone
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCS(=O)(=O)c1cccnc1Oc1ccc(C(=O)c2ccccc2)cc1
Reaction #372447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc2nccc(Oc3ccc(C(=O)c4ccccc4)cc3)c2cc1OC
Reaction #391136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
NS(=O)(=O)Oc1ccc(C(=O)c2ccccc2)cc1
Reaction #414891
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
O=C(c1ccccc1)c1ccc(CP(=O)(Cl)Cl)cc1
Reaction #424580
(4-benzoylbenzyl)phosphonic dichloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C=CCOc1ccc(C(=O)c2ccccc2)cc1
Reaction #445563
4-allyloxybenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
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