Recherche de Sous-structure

3493

COc1ccc(CCN=C=O)cc1
Reaction #2933
4-methoxy-β-phenylethyl isocyanate
Rendement 0.1%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2c(c1)CCO2
Reaction #3097
title compound
Rendement 60.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cccc(Cl)c2c(=O)o1
Reaction #3197
title compound
Rendement 250.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2[nH]c(=O)oc(=O)c12
Reaction #3209
title compound
Rendement 283.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(C(F)(F)F)cc(Cl)c2c(=O)o1
Reaction #3226
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)C(F)(Cl)Oc1ccc(Cl)cc1
Reaction #4836
4-(1-chloro-1,2,2,2-tetrafluoroethoxy)chlorobenzene
Rendement 89.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(O)(C(F)(F)F)C(F)(F)F)ccc1C=O
Reaction #4846
2-methoxy-4-[2,2,2-trifluoro-1-hydroxy-(trifluoromethyl)ethyl]benzaldehyde
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(C)c2[nH]c(=O)[nH]c12
Reaction #5331
title compound
Rendement 4777.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(F)c(I)cc2c(=O)o1
Reaction #6918
title compound
Rendement 90.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(C=O)cc1OC
Reaction #6993
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10029
pure compound
Rendement 70.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10030
pure compound
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10031
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10033
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10035
product
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)N4CCCCC4)c3C2=O)C(=O)N1
Reaction #10153
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4- yl]methyl}piperidylcarboxamide
Rendement 145.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nn1c(=O)c2cc(F)c(F)c(Cl)c2n(C2CC2)c1=O
Reaction #10407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(F)c(F)cc2c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10409
title compound
Rendement 198.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2nc3cccnc3[nH]2)cc1C=O
Reaction #10795
5-(3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethoxy-benzaldehyde
Rendement 64.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2c[nH]c(C3CC3)n2)cc1C=O
Reaction #10825
5-(2-cyclopropyl-1H-imidazol-4-yl)-2,4-dimethoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
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