2-chlorobenzaldehyde

CCOC(=O)C1=C(CCl)N2CCOC2(C)C(C(=O)OC)C1c1ccccc1Cl
Reaction #1350
title compound
Ausbeute 17.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C(=Cc2ccccc2Cl)N2CCC1CC2
Reaction #5074
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #9099
yield
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #43776
solid
Ausbeute 289.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C(=Cc1ccccc1Cl)C(=O)COCCN1C(=O)c2ccccc2C1=O
Reaction #53754
Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
OC(c1ccc(Cl)cc1)c1ccccc1Cl
Reaction #56541
2,4'-dichlorobenzhydrol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C1CC(c2ccccc2Cl)Oc2ccc(O)cc21
Reaction #59563
2-(2-Chlorophenyl)-6-hydroxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)NCc1ccccc1Cl
Reaction #61328
(2-Chlorobenzyl)isopropylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)C=Cc1ccccc1Cl
Reaction #74771
4-(2-chlorophenyl)-but-3-ene-2-one
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Cc1c(Cl)cccc1N=Cc1ccccc1Cl
Reaction #75365
N-(o-chlorobenzylidene)-3-chloro-2-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C1CC(=O)CC(c2ccccc2Cl)C1
Reaction #77460
5-(2-chlorophenyl)cyclohexane-1,3-dione
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cl.OC1(c2ccccc2Cl)C(c2ccccc2Cl)SC2=NCCCCN21
Reaction #95511
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
OC1(c2cccs2)C(c2ccccc2Cl)SC2=NCCCCN21
Reaction #95515
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Clc1ccccc1-c1nc2cc(-c3nc4ccccc4o3)ccc2n1C1CCOCC1
Reaction #161489
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(C=Cc1ccccc1Cl)C=Cc1ccccc1Cl
Reaction #164843
yellow solid
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CC(O)c1ccccc1Cl
Reaction #176338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c3c(c(=O)oc2c1)CN(Cc1ccccc1Cl)CC3
Reaction #182726
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(N)c(C(=O)c2ccccc2Cl)cc1C
Reaction #183665
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(=O)C(=Cc1ccccc1Cl)C(=O)OCC
Reaction #186720
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cccc(NCc2ccccc2Cl)n1
Reaction #189644
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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