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CCOC(=N)Cc1ccc(F)cc1

N=C(Cc1ccc(F)cc1)Nc1ncccc1OCc1ccccc1
Reaction #230690
DOI: 10.1039/C8SC04228D
CCOC(=N)C(O)c1ccc(F)c(Br)c1
Reaction #238914
DOI: 10.1039/C8SC04228D
Cl
Reaction #254624
DOI: 10.1039/C8SC04228D
CCOC(=N)C(O)c1ccc(F)c(Br)c1.Cl
Reaction #359840
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccc(F)c(Br)c1)C1NC=CCN1
Reaction #359841
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #766926
DOI: 10.1039/C8SC04228D
CCOC(=N)Cc1ccc(F)cc1.Cl
Reaction #805326
ethyl 2-(4-fluorophenyl)acetimidate hydrochloride
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N=C(Cc1ccc(F)cc1)OCC
Reaction #805327
ethyl N-ethoxycarbonyl-2-(4-fluorophenyl)acetimidate
Ausbeute 52.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)Cc1ccc(F)cc1.Cl
Reaction #1741997
Ethyl 4-fluorophenylacetimidate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N=C(Cc1ccc(F)cc1)Nc1ncccc1OCc1ccccc1
Reaction #1741998
product
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1COc1cccnc1NC(=N)Cc1ccc(F)cc1.Cl
Reaction #1742003
product
Ausbeute 5.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)Cc1ccc(F)cc1F.Cl
Reaction #1977964
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(Cc1ccc(F)cc1F)=NC#N
Reaction #1977965
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1COc1cccnc1NC(=N)Cc1ccc(F)cc1
Reaction #2246334
DOI: 10.1039/C8SC04228D