p-hydroxybenzoic acid

CCCCCCCCCC(=O)Oc1ccc(C(=O)O)cc1
Reaction #848
p-decanoyloxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #849
acid chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C)COC(=O)c1ccc(O)cc1
Reaction #6410
ester
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(C)CCOC(=O)c1ccc(O)cc1
Reaction #6413
ester
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(C)COC(=O)c1ccc(O)cc1
Reaction #6414
ester
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccc(O)cc1
Reaction #6509
4-Hydroxy-4'-nitrobenzanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccc(O)cc1
Reaction #6514
4-Hydroxy-4'-nitrobenzanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)c1ccc(OC2CCCCO2)cc1
Reaction #7427
p-tetrahydropyranyloxy benzoic acid
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(OCCCCCCO)cc1
Reaction #10214
4-(6-hydroxyhexyloxy)-benzoic acid
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCOCCOc1ccc(C(=O)O)cc1
Reaction #11500
title compound
Ausbeute 105.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)Oc1ccc(C(=O)O)cc1
Reaction #54997
4-acetoxy benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(OCc1ccccc1)c1ccc(OCc2ccccc2)cc1
Reaction #81358
phenylmethyl 4-(phenylmethoxy)benzoate
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(C)OC(=O)c1ccc(O)cc1
Reaction #81549
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #84197
Formula 4
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[Si](C)(C)Oc1ccc(C(=O)O)cc1
Reaction #90241
4-tert-butyldimethylsilyloxybenzoic acid
Ausbeute 53000.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccc(O)cc1
Reaction #90245
21
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCC(C)(C)c1ccc2oc(-c3ccc(O)cc3)nc2c1
Reaction #159254
product
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1ccc(O)cc1)c1ccc(OCCBr)cc1
Reaction #176770
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Oc1ccc(C(=O)O)cc1
Reaction #177072
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(O)cc1)N1CCCC2c3ccccc3CC21
Reaction #178391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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