Busqueda de Subestructura

108104

COc1nc(Nc2cc(C(F)(F)F)ccc2F)ncc1Br
Reaction #761
Rendimiento 0.0%
COc1nc(Nc2cc(C(F)(F)F)ccc2F)ncc1Br
Reaction #825
Rendimiento 84.9%
COc1nc(Nc2cc(C(F)(F)F)ccc2F)ncc1Br
Reaction #826
Rendimiento 80.8%
COc1cccc(-c2ccc(F)c([N+](=O)[O-])c2)c1
Reaction #11632
4-fluoro-3′-methoxy-3-nitro-biphenyl
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)c(F)c([N+](=O)[O-])c1OC
Reaction #45798
compound
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)c(F)c(N)c1OC
Reaction #45799
compound
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N(c1ccc(N2CN=c3sccc3=C2N)cc1)c1cc(C(F)(F)F)ccc1F
Reaction #60768
4-Amino-3-(4-((2-fluoro-5-(trifluoromethyl)phenyl)-aminocarbonylamino)phenyl)thieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Nc1cc(C(F)(F)F)ccc1F)c1ccc(N2CN=c3sccc3=C2N)cc1
Reaction #60770
4-Amino-3-(4-((2-fluoro-5-(trifluoromethyl)phenyl)-aminocarbonyl(N-methylamino))phenyl)thieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(F)c([N+](=O)[O-])cc1C
Reaction #62314
title compound
Rendimiento 57.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc([N+](=O)[O-])c(F)cc1N
Reaction #62315
title compound
Rendimiento 95.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc(F)c([N+](=O)[O-])c2)c1
Reaction #77407
4-fluoro-3′-methoxy-3-nitrobiphenyl
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)c(F)c2nn[nH]c12
Reaction #158136
5-Bromo-4-fluoro-7-methyl-1H-benzotriazole
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2ncc3c(=O)[nH]c4cc(C(=O)N(C)C)ccc4n23)c1
Reaction #159910
title compound
Rendimiento 8.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-n2ccnc2-c2ccsc2)c([N+](=O)[O-])c1
Reaction #159935
N,N-dimethyl-3-nitro-4-[2-(3-thienyl)-1H-imidazol-1-yl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc([N+](=O)[O-])c(F)cc1OCC
Reaction #159945
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c([N+](=O)[O-])cc1C(C)=O
Reaction #159950
title compound
Rendimiento 92.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1[N+](=O)[O-]
Reaction #160614
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1[N+](=O)[O-]
Reaction #160618
title compound
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2nc3ccccc3o2)cc(C(F)(F)F)c1F
Reaction #161458
title compound
Rendimiento 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1ccc(F)c(NS(C)(=O)=O)c1
Reaction #163135
N-[5-(1-Aminoethyl)-2-fluorophenyl]methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
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