4-hydroxy-3-methoxybenzaldehyde

COc1cc(C=O)ccc1OCCCCCCCCCCOc1ccc(C=O)cc1OC
Reaction #6290
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(C=O)cc(Br)c1O
Reaction #43600
desired compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CCN1CCC(C(=O)OC)CC1
Reaction #44337
1-Prop-2-ynyl-piperidine-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(C=O)ccc1S(=O)(=O)N(C)C
Reaction #48232
4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)CCCOc1ccc(C=O)cc1OC
Reaction #62264
keto-ester
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(C=O)ccc1OCCOC(C)=O
Reaction #66992
title compound
Rendement 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(/C=C(\C#N)c2ccc(C(F)(F)F)nc2)ccc1O
Reaction #70925
(Z)-3-(4-hydroxy-3-methoxyphenyl)-2-(6-(trifluoromethyl)pyridin-3-yl)acrylonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #72725
solid
Rendement 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(C=O)ccc1O[C@H]1CCN(C(=O)OC(C)(C)C)C1
Reaction #82270
title compound
Rendement 77.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cc(C=O)ccc1OCCCCl
Reaction #83911
4-(3-chloropropoxy)-3-methoxybenzaldehyde
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cc(C=CC(=O)c2ccccc2O)ccc1O
Reaction #90239
2′,4-dihydroxy-3-methoxychalcone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(/C=C(\C#N)c2ccc(C(F)(F)F)nc2)ccc1O
Reaction #90271
(Z)-3-(4-hydroxy-3-methoxyphenyl)-2-(6-(trifluoromethyl)pyridin-3-yl)acrylonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(C=O)ccc1OS(=O)(=O)C(F)(F)F
Reaction #157504
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(C=O)ccc1C(=O)CCCCCBr
Reaction #160689
product 44
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCOc1ccc(C=O)cc1OC
Reaction #164815
white solid
Rendement 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(C=O)ccc1OCCOC(C)=O
Reaction #167190
title compound
Rendement 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(C=O)ccc1OCCN(C)C
Reaction #173558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C2NCCS2)ccc1O
Reaction #175096
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc(C=O)cc1OC
Reaction #175272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1Cc2c([nH]c3ccccc23)C(c2ccc(O)c(OC)c2)N1
Reaction #176067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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