Busqueda de Subestructura

1217024

COC(=O)/C(C#N)=C(\C)c1ccc2c(c1)CCO2
Reaction #51208
title product
Rendimiento 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #62747
orange solid
Rendimiento 66.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #62748
Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnccc1CNS(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78006
title compound
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CC(=O)O)CC(=O)O)c1
Reaction #78007
title compound
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)c2ccc(C(=O)O)cc2)c1
Reaction #78008
title compound
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CCC(=O)O)Cc2ccccc2)c1
Reaction #78009
title compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C1CCN(Cc2ccccc2)C1)S(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78011
title compound
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)C2CCN(C)CC2)c1.Cl.Cl
Reaction #78012
title compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)Cc2cccnc2)c1.Cl.Cl
Reaction #78013
title compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C#N)=C/c1ccc(Oc2ccccc2)cc1
Reaction #168222
(E)-ethyl 2-cyano-3-(4-phenoxyphenyl)acrylate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccc(Oc3ccccc3)cc2)nc(-c2ccccc2)[nH]c1=O
Reaction #168223
6-oxo-4-(4-phenoxyphenyl)-2-phenyl-1,6-dihydropyrimidine-5-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=Cc1ccc(OCCc2nc(-c3ccccc3Cl)oc2C)cc1
Reaction #208692
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C#N)Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #247616
DOI: 10.1039/C8SC04228D
CC(C)(C)COC(=O)C(C#N)=Cc1cc(O)c(O)c([N+](=O)[O-])c1
Reaction #258346
DOI: 10.1039/C8SC04228D
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)c2ccc(C(=O)O)cc2)c1
Reaction #259470
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)c(OCCOc2ccc(C=C(C#N)C(=O)O)cc2)c(Cl)c1
Reaction #266061
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C#N)=Cc1ccc(OCCc2nc(-c3ccccc3Cl)oc2C)cc1
Reaction #320468
ethyl 4-[2-[2-(2-chlorophenyl)-5-methyl-4-oxazolyl]ethoxy]-α-cyanocinnamate
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)Cc1ccc(OCCc2nc(-c3ccccc3Cl)oc2C)cc1
Reaction #320469
ethyl 3-[4-[2-[2-(2-chlorophenyl)-5-methyl-4-oxazolyl]ethoxy]phenyl]-2-cyanopropionate
Rendimiento 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=C(C)c1ccc(OC)cc1
Reaction #357381
2-Cyano-3-(4-methoxyphenyl)-but-2-enoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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