5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde

N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
Reaction #6992
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #586184
desired product
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #1230920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #1321595
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=Cc1cc(-c2ccccc2)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #1445566
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
O=Cc1cccc(-c2ccccn2)c1
Reaction #1445567
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
Reaction #1445568
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #1445569
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #1541407
desired product
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
Reaction #1926608
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_01
O=Cc1cc(-c2ccccc2)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #2275445
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
O=Cc1cccc(-c2ccccn2)c1
Reaction #2275446
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
Reaction #2275447
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
CNCc1cc(Br)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #2275448
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
O=Cc1cc(-c2ccccc2)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #2405639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)