3-chlorobenzaldehyde

CCC1CN(c2ccc(F)c(C(F)(F)F)c2)C(c2cccc(Cl)c2)O1
Reaction #4218
2-m-Chlorophenyl-3-(3-trifluoromethyl-4-fluorophenyl)-5-ethyl oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])C=Cc1cccc(Cl)c1
Reaction #6489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2ccccc2C(=O)N1CC/C=C\c1cccc(Cl)c1
Reaction #6813
cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(C)C(c1cccc(Cl)c1)c1cn(C)c2ccccc12
Reaction #9144
[(3-Chloro-phenyl)-(1-methyl-1H-indol-3-yl)-methyl]-dimethyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2Cc3c(NCc4cccc(Cl)c4)cccc3C2=O)C(=O)N1
Reaction #10149
product
Ausbeute 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(-c2cccc(Cl)c2)n1-c1ccc(S(=O)(=O)N2CCCCC2)cc1
Reaction #46931
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cccc(CNc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #51565
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(O)C=Cc1cccc(Cl)c1
Reaction #54246
3-chlorocinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C1CC(c2cccc(Cl)c2)Oc2ccc(O)cc21
Reaction #59461
2-(3-Chlorophenyl)-6-hydroxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Clc1cccc(CNC2CC2)c1
Reaction #61346
(3-Chlorobenzyl)cyclopropylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Clc1cccc(CNc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #75855
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(=O)OCCCn1c(=O)c([N+](=O)[O-])c(/C=C/c2cccc(Cl)c2)n(C)c1=O
Reaction #88624
(E)-3-(4-(3-chlorostyryl)-3-methyl-5-nitro-2,6-dioxo-2,3-dihydropyrimidin-1 (6H)-yl)propyl acetate
Ausbeute 16.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Clc1cccc(-c2nc3cc(-c4nc5ccccc5o4)ccc3n2C2CCOCC2)c1
Reaction #161490
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)Cn1c(-c2cccc(Cl)c2)nc2ccc(N3CCN4CCC3CC4)cc2c1=O
Reaction #164560
2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-(3-chlorophenyl)-4-oxoquinazolin-3(4H)-yl)acetic acid
Ausbeute 44.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1c(-c2cccc(Cl)c2)nc2ccc(O)cc2c1=O
Reaction #164580
2-(3-chlorophenyl)-6-hydroxy-3-methylquinazolin-4(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(C=Cc1cccc(Cl)c1)C=Cc1cccc(Cl)c1
Reaction #164842
yellow solid
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O/N=C\c1cccc(Cl)c1
Reaction #170396
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCCCCCc1noc(-c2ccc(CNCc3cccc(Cl)c3)cc2)n1
Reaction #190706
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1cccc(C2OCCCO2)c1
Reaction #195699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])CC(O)c1cccc(Cl)c1
Reaction #200585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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