Substructure Search

CCN=C=O

C=C(C)C(=O)OCCNC(=O)Nc1ccc(O)cc1
Reaction #2773
2-(N'-(4-hydroxyphenyl)ureido)ethylmethacrylate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCNC(=O)OCc1ccccc1
Reaction #3173
benzyloxycarbonylaminoethyl methacrylate
Yield 80.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CCCNc2ncc3cc(-c4c(Cl)cccc4Cl)c(NC(=O)NCc4ccccc4)nc3n2)CC1
Reaction #3522
1-benzyl-3-{6-(2,6-dichlorophenyl)-2-[3-(4-methyl-piperazin-1-yl)-propylamino]-pyrido[2,3-d]pyrimidin-7-yl}-urea
Yield 63.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=O)c1ccccc1[N+](=O)[O-])Nc1ccc(Oc2ncc(Br)cn2)c(Cl)c1
Reaction #4609
desired product
Yield 84.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C=NCc1ccccc1OCc1ccccc1
Reaction #4631
2-benzyloxybenzyl isocyanate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)NCc1ccccc1OCc1ccccc1
Reaction #4632
N-(2-hydroxyethyl)-N'-(2-benzyloxybenzyl)urea
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
Reaction #4709
N-Benzyl-2-[[3-[3-(1-piperidinylmethyl)phenoxy]propyl]aminothioxomethyl]-hydrazine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCOc1cccc(CN2CCCCC2)c1)NNC(=O)NCc1ccccc1
Reaction #4718
N-Benzyl-N'-[3-[3-(1-piperidinylmethyl)-phenoxy]propyl]1,2-hydrazine dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCCNC(=O)N(CCO)CCO
Reaction #4790
2-[N',N'-Bis(2-hydroxyethyl)ureido]ethyl Methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
N#CCN(C(=O)NC(=O)c1c(Cl)cccc1Cl)c1ccc(Cl)cc1
Reaction #5727
N-(2,6-dichlorobenzoyl)-N'-(cyanomethyl)-N'-(p-chlorophenyl)-urea
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(-c2ccco2)c2cnn(C(=O)NCc3ccccc3)c2n1
Reaction #8399
title compound
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)NCc4ccccc4)c3C2=O)C(=O)N1
Reaction #10122
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(benzylamino)carboxamide
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)Nc1nc(-c2ccco2)c2ccnc-2[nH]1
Reaction #11852
title compound
Yield 19.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)N(c2cccc(NC(=O)NCc3ccccc3)c2)C1
Reaction #51180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccccc1)OCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52010
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccccc1)OCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)OCC2CCC(CN(Cc3ccccc3)S(=O)(=O)NC(=O)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)CC2)c1
Reaction #52012
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cc2cc(OCCCNC(=O)NCc3ccccc3)ccc2[nH]1
Reaction #52265
title compound
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C=NC(=O)c1c(F)cccc1F
Reaction #54814
2,6-difluorobenzoyl isocyanate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1nc(-c2c(F)cccc2F)oc(=O)n1-c1ccc(Cl)c(Cl)c1
Reaction #54815
3-(3,4-dichlorophenyl)-6-(2,6-difluorophenyl)-3,4-dihydro-2H-1,3,5-oxadiazin-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
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