Busqueda de Subestructura

CC(C)N(CCCl)C(C)C.Cl

CC(C)N(CCN1C(=O)c2ccccc2C1=O)C(C)C.Cl
Reaction #4298
white crystalline product
Rendimiento 62.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1Cc2ccccc2C(C)N1C(=O)C(Cl)Cl
Reaction #273078
DOI: 10.1039/C8SC04228D
CC1(C)OC(c2ccc(S(C)(=O)=O)cc2)C(CF)N1C(=O)C(Cl)Cl
Reaction #274355
DOI: 10.1039/C8SC04228D
CC1Cc2ccccc2C(C)N1C(=O)C(Cl)Cl
Reaction #318576
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2ccccc2CC(C)N1C(=O)C(Cl)Cl
Reaction #318577
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1
CCC1Cc2ccccc2C(C)N1C(=O)C(Cl)Cl
Reaction #318578
2-(Dichloroacetyl)-1-methyl-3-ethyl-1,2,3,4-tetrahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CC(C)N(C(=O)CN=[N+]=[N-])C(C)C2)c(F)cc2c(=O)c(C(=O)NCc3ccc(Cl)cc3Cl)cn(C3CC3)c12.Cl
Reaction #339040
7-[(3RS,5SR)-4-(Azidoacetyl)-3,5-dimethylpiperazin-1-yl]-1-cyclopropyl-N-(2,4-dichlorobenzyl)-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2ccccc2C(C)N1C(=O)C(Cl)Cl
Reaction #369295
DOI: 10.1039/C8SC04228D
CC(C)N(C(=O)C(Cl)Cl)C(C)C
Reaction #391696
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)c(N1CCN(C(=O)c3cccs3)CC1)c(C#N)c(=O)n2CCN(C)C
Reaction #433823
pale yellow solids
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1C(c2ccccc2)OC(C)(C)N1C(=O)C(Cl)Cl
Reaction #522238
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H](c2ccc(S(C)(=O)=O)cc2)[C@@H](CO)N1C(=O)C(Cl)Cl
Reaction #595072
(4R,5R)-3-dichloroacetyl-2,2-dimethyl-4-hydroxymethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H](c2ccc(S(C)(=O)=O)cc2)[C@@H](CF)N1C(=O)C(Cl)Cl
Reaction #595073
(4S,5R)-3-dichloroacetyl-2,2-dimethyl-4-fluoromethyl-5-[4-(methylsulfonyl)phenyl]-1,3-oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc([C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl)cc1
Reaction #595074
(1R,2S)-2-dichloroacetamido-3-fluoro-1-[4-(methylsulfonyl)phenyl]-1-propanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H]2OC(C)(C)N(C(=O)C(Cl)Cl)[C@@H]2CF)cc1
Reaction #612694
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1noc(-c2ccc([C@H]3OC(C)(C)N(C(=O)C(Cl)Cl)[C@@H]3CF)cc2)n1
Reaction #612695
title compound
Rendimiento 38.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@H](c2ccc(-c3ccc(CO)nc3)cc2)[C@@H](CF)N1C(=O)C(Cl)Cl
Reaction #612702
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H](CF)[C@H](O)c1ccc(-c2ccc(CN3CCC3)nc2)cc1)C(Cl)Cl
Reaction #612703
title compound
Rendimiento 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NCc1ccc(-c2ccc([C@H]3OC(C)(C)N(C(=O)C(Cl)Cl)[C@@H]3CF)cc2)cn1
Reaction #612705
title compound
Rendimiento 43.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)nc(NCCN(C(C)C)C(C)C)n1
Reaction #701490
2-(2-Diisopropylaminoethylamino)-4, 6-dimethyl pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente