2-ethylphenol

—
Reaction #9766
filtrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1cc(SC#N)ccc1O
Reaction #157263
3-ethyl-4-hydroxy-phenyl thiocyanic acid
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1cccc([N+](=O)[O-])c1O
Reaction #174645
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1ccccc1OCCCCBr
Reaction #175087
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(Br)ccc1O
Reaction #205954
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(Br)ccc1O
Reaction #236154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1cc(Br)ccc1O
Reaction #241348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1cccc(Br)c1O
Reaction #251723
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1ccccc1OCc1ccccc1
Reaction #265440
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCc1ccccc1
Reaction #268247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1cc(C=O)ccc1O
Reaction #292781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1cccc(C=O)c1O
Reaction #305425
9
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCc1cccc(O)c1
Reaction #318850
m-ethylphenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCOC(=O)COc1ccccc1CC
Reaction #357328
product
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCc1cc(C(C)=O)ccc1O
Reaction #484018
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCc1cc(Br)ccc1O
Reaction #484043
title compound
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCc1cccc([N+](=O)[O-])c1O
Reaction #487782
2-ethyl-6-nitrophenol
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C=Cc1ccc(O)cc1
Reaction #523908
p-vinylphenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
C=Cc1ccc(O)cc1
Reaction #523909
p-vinylphenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
CCc1ccccc1OCC(C)N1C(=O)c2ccccc2C1=O
Reaction #566169
2-[2-(2-ethylphenoxy)-1-methylethyl]-1H-isoindole-1,3(2H)-dione
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
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