3-ethoxy-4-hydroxybenzaldehyde

CCOc1cc(C=CC(C)=O)ccc1O
Reaction #66945
yellow crystal
Rendement 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOc1cc(C=CC(=O)O)ccc1O
Reaction #82110
compound
Rendement 56.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOc1cc(C=O)cc([N+](=O)[O-])c1O
Reaction #211516
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1cc(C=O)ccc1Oc1ccc(C#N)cn1
Reaction #217977
title compound
Rendement 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOc1cc(CNCCC(C)C)ccc1Oc1ccc(C(N)=O)cc1
Reaction #218087
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOc1cc(C=O)ccc1OCCO
Reaction #231236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(C=C2CCN(C(N)=O)C2=O)ccc1O
Reaction #239201
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(CN2CCC(NC(=O)c3cncc(C)c3)CC2)ccc1O
Reaction #246645
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(C=O)ccc1OCC=C(C)C
Reaction #259036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1cc(C=O)ccc1OC(C)C
Reaction #262767
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOc1cc(C=O)cc([N+](=O)[O-])c1O
Reaction #276518
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C(C)COc1ccc(C=O)cc1OCC
Reaction #300071
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOc1cc(C=O)ccc1Oc1ccc(C#N)cn1
Reaction #315435
title compound
Rendement 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCOc1cc(CNCCC(C)C)ccc1Oc1ccc(C(N)=O)cc1
Reaction #315540
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCOc1cc(C=C2SC(=S)N(N(C)C)C2=O)ccc1O
Reaction #361073
subtitled intermediate
Rendement 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCOc1cc(CN2CCCC2)ccc1O
Reaction #373548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOc1cc(C=CC(C)=O)ccc1O
Reaction #388868
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)C(=O)O.CCOc1cc(C=O)ccc1O
Reaction #450469
ethylvanillin isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CC(C)C(=O)O.CCOc1cc(C=O)ccc1O
Reaction #450470
ethylvanillin isobutyrate
Rendement 71.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
O=Cc1ccc(O)c(O)c1
Reaction #452409
3,4-dihydroxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Page 1Suivant