2-hydroxy-p-tolualdehyde

O=Cc1ccccc1O
Reaction #452408
o-hydroxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCOc1cc(C=O)ccc1C
Reaction #635126
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CCOc1cc(C=O)ccc1C
Reaction #1000303
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CCOc1cc(C=O)ccc1C
Reaction #1000506
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CCCCCC=Cc1ccc(C)c(O)c1
Reaction #1302267
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCOc1cc(C=O)ccc1C
Reaction #1802333
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
CCOc1cc(C=O)ccc1C
Reaction #2214441
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCOc1cc(C=O)ccc1C
Reaction #2330179
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03
CCOc1cc(C=O)ccc1C
Reaction #2351649
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
CCCCC/C=C\c1ccc(C)c(O)c1
Reaction #2353598
title compound
Rendimiento 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
CCOc1cc(C=O)ccc1C
Reaction #2442774
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_07
CCOc1cc(C=O)ccc1C
Reaction #2513764
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_06