Substructure Search

933619

CCOC(=N)c1cc(Cl)ccc1OC
Reaction #56828
5-chloro-2-methoxy-benzimidic acid ethyl ester
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)c1cc(Cl)ccc1OC.Cl
Reaction #163476
title compound
Yield 101.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Cl)ccc1Oc1cccc(O)c1
Reaction #182858
DOI: 10.1039/C8SC04228D
N#Cc1cc(Cl)ccc1OCc1ccccc1Br
Reaction #201045
DOI: 10.1039/C8SC04228D
N#Cc1cc(Cl)ccc1OCC(F)(F)F
Reaction #209241
DOI: 10.1039/C8SC04228D
N#Cc1cc(Cl)cc2c1OC(C(F)(F)F)C(C(=O)O)=C2
Reaction #231125
DOI: 10.1039/C8SC04228D
N#Cc1cc(Cl)ccc1OC(OCc1ccccc1)C(=O)c1ccccc1
Reaction #239051
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(n2ncc3c(Oc4ccc(Cl)cc4C#N)ncnc32)CC1
Reaction #296245
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)O)c(Cl)cc1C#N
Reaction #307058
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC)c(C#N)cc1Cl
Reaction #307059
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)c1cc(Cl)ccc1OC.Cl
Reaction #340837
title compound
Yield 101.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)c1cc(Cl)ccc1OC.Cl
Reaction #341860
title compound
Yield 101.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NCC(O)COc1ccc(Cl)cc1CN
Reaction #346486
1-(2-aminomethyl-4-chlorphenoxy)-2-hydroxy-3-tert.-butylamino propane
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(Cl)cc1C#N
Reaction #368705
DOI: 10.1039/C8SC04228D
—
Reaction #456602
solid
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccccc1N1NN=C(Cl)N1)c1nnc(-c2ccccc2C(F)(F)F)n1C
Reaction #476300
5-chloro-2-[(1S)-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy phenyl}-1H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(Cl)cc1C=O)c1nnc(-c2ccccc2C(F)(F)F)n1C.Cl
Reaction #476301
5-chloro-2-[(1S)-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy]benzaldehyde monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(-c2ccc(OCCO)cc2Br)nnc1C(C)(C)Oc1ccc(Cl)cc1C(=O)O
Reaction #476314
2-(1-{5-[2-bromo-4-(2-hydroxyethoxy)phenyl]-4-methyl-4H-1,2,4-triazol-3-yl}-1-methylethoxy)-5-chlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(Cl)cc1CN
Reaction #480086
title compound
Yield 630.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCc1cc(Cl)ccc1OCCN1CCOCC1
Reaction #480087
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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