methyl p-hydroxybenzoate

C=CCOc1ccc(C(=O)OC)cc1
Reaction #3072
methyl 4-allyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOCCCCCCCCCCOc1ccc(C(=O)O)cc1
Reaction #5259
4-(10-allyloxydecyloxy)benzoic acid
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49711
methyl 4-octadecyloxybenzoate
Ausbeute 45.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49714
Methyl 4-dodecyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCCCCCCCCCCCCCCCCCCCCCOc1ccc(C(=O)OC)cc1
Reaction #49716
Methyl 4-docosyloxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51654
4-(4-fluorophenoxy)benzoic acid
Ausbeute 91.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1ccc(OCCN)cc1.Cl
Reaction #57989
4-(2-aminoethoxy)benzoic acid methyl ester hydrochloride
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1ccc(OCc2ccc3ccccc3n2)cc1
Reaction #62097
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOc1ccc(C(=O)OC)cc1
Reaction #63009
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)c1ccc(O)cc1.O
Reaction #64271
Methyl Paraben·H2O
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)c1ccc(O)c(Br)c1
Reaction #69449
methyl 3-bromo-4-hydroxybenzoate
Ausbeute 106.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(O)c(C(CCN(C(C)C)C(C)C)c2ccccc2)c1
Reaction #69938
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1ccc(OCCCCc2ccccc2)cc1
Reaction #80885
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1ccc(OC(F)(F)C(F)C(F)(F)F)cc1
Reaction #94923
4-(1,1,2,3,3,3-hexafluoropropyloxy)-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COC(=O)c1ccc(OCCCCCO)cc1
Reaction #155823
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(OCCC(C)CCCC(C)C)cc1
Reaction #171242
title compound
Ausbeute 95.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(OCc2ccccc2)cc1
Reaction #174840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OCC2CC(Oc3ccc(F)cc3F)CN2C(=O)OC(C)(C)C)cc1
Reaction #177141
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OCc2ccccn2)cc1
Reaction #182556
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOc1ccc(C(=O)OC)cc1
Reaction #189718
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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