4-Chloromethylbenzoic acid

COC(=O)C1(NC(=O)c2ccc(CCl)cc2)CCCCC1
Reaction #161038
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(C2COCCOC2)c2sc(NC(=O)c3ccc(CCl)cc3)nc12
Reaction #244833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(CCl)cc1
Reaction #268065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl
Reaction #283304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)CCNC(=O)c1ccc(CCl)cc1
Reaction #395683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cl)c1ccc(CCl)cc1
Reaction #440993
4-(chloromethyl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COC(=O)C1(NC(=O)c2ccc(CCl)cc2)CCCCC1
Reaction #535945
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(O)c1ccc(CSc2nnc(-c3ccc4c(c3)CCO4)o2)cc1
Reaction #539879
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCN(CC)Cc1ccc(C(=O)O)cc1
Reaction #575723
α-diethylamino-paratoluic Acid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
O=C(O)c1ccc(CN2CCCNCCNCCCNCC2)cc1
Reaction #594978
title compound
Ausbeute 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(Cl)c1ccc(CCl)cc1
Reaction #833677
4-(chloromethyl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
O=C(O)c1ccc(COc2ccccc2)cc1
Reaction #912051
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)CCCNC(=O)c1ccc(CCl)cc1
Reaction #917410
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)OC(=O)c1ccc(CCl)cc1
Reaction #922925
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)OC(=O)c1ccc(CCl)cc1
Reaction #975231
benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCOC(=O)CCNC(=O)c1ccc(CCl)cc1
Reaction #975232
compound 13f
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCOC(=O)CCCNC(=O)c1ccc(CCl)cc1
Reaction #975233
compound 13g
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCN(CC)CCN(C)Cc1ccc(C(=O)O)cc1
Reaction #1014059
4-(((2-(diethylamino)ethyl)(methyl)amino)methyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(O)c1ccc(COc2ccccc2)cc1
Reaction #1057964
4-phenoxymethylbenzoic acid
Ausbeute 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
OCc1ccc(CCl)cc1
Reaction #1057984
4-chloromethylbenzyl alcohol
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
Seite 1Weiter