4-Hydroxyphenylacetic acid

O=C(Cc1ccc(O)cc1)OCc1ccccc1
Reaction #2320
benzyl 4-hydroxyphenylacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #3086
3-[((4-chloroanilino) carbonyl)methyl]phenol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #6538
3-[((4-chloroanilino) carbonyl)methyl]phenol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)Cc1ccc(O)cc1
Reaction #76424
methyl(4-hydroxyphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc(/C=C/c2ccc(O)cc2)cc(OC)c1
Reaction #87291
pterostilbene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Cc1ccc(O)cc1)ON1C(=O)CCC1=O
Reaction #201939
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(Oc2ccc(CC(=O)O)cc2)cc1
Reaction #207781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)Cc1ccc(OCc2ccccc2C(=O)O)cc1
Reaction #223198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2c(Oc3ccc(CC(=O)O)cc3)ncnc2cc1OCCOC1CCCCO1
Reaction #231702
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc(C(O)CNC(=O)Cc2ccc(O)cc2)cs1
Reaction #232872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)COC(=O)Cc1ccc(O)cc1
Reaction #244209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccccc1COc1ccc(CC(=O)O)cc1
Reaction #278570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(COc1ccc(CC(=O)O)cc1)OCC
Reaction #288466
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1ccc(NC(=O)Cc2ccc(O)cc2)cc1
Reaction #300594
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)Cc1ccc(O)c(CCl)c1
Reaction #312489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
O=C(O)C(C(=O)O)c1ccc(O)cc1
Reaction #312490
α-carboxy-4-hydroxybenzeneacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #320532
3-[((4-chloroanilino) carbonyl)methyl]phenol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCCCCCCCCCCCOc1ccc(CC(=O)O)cc1
Reaction #322870
desired title compound
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=C(Cc1ccc(O)cc1)OCCC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #350989
3,3,3-Triphenylpropyl 2-(4-hydroxyphenyl)acetate
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
O=C(Cc1ccc(O)cc1)OCc1ccccc1
Reaction #353927
benzyl 4-hydroxyphenylacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
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