Busqueda de Subestructura

C(CCBr)CCl

O=C(CCCBr)Nc1ccccc1Cc1ccccc1
Reaction #1051
2-benzyl-1-(4-bromobutyrylamino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[N-]C(C)C.[Li+]
Reaction #1296
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[N-]C(C)C.[Li+]
Reaction #1432
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCBr)N1CC(c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5923
4-(4-bromobutyryl)-2-(4-chlorophenyl)-3,4-dihyro-2H-1,4-benzothiazine
Rendimiento 93.2%DOI: 10.6084/m9.figshare.5104873.v1
ClCCCCSc1ccccn1
Reaction #6268
desired compound
Rendimiento 65.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N(CCCCCl)c1ccccc1N(CCCCCl)C(=O)CC
Reaction #6282
desired product
Rendimiento 12.6%DOI: 10.6084/m9.figshare.5104873.v1
ClCCCCSc1ccncc1
Reaction #6286
desired compound
Rendimiento 89.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1c(I)cc(I)cc1I)C(F)(F)C(F)(Br)C(F)(F)Br
Reaction #6407
material
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1c(I)cc(I)c(Br)c1I)C(F)(F)C(F)(Br)C(F)(F)Br
Reaction #6408
(2,4,6-triiodo-3-bromo-phenyl)-2,2,3,4,4-pentafluoro-3,4-dibromobutyrate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)CC(CBr)Cc1ccccc1
Reaction #8315
3-benzyl-4-bromo-butyryl chloride
Rendimiento 127.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CBr)Cc1ccccc1)NN=C(Cc1ccnc2ccccc12)c1ccccn1
Reaction #8316
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C1=CNc1ccc(OCCCCCl)cc1
Reaction #11588
compound
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(CCCCCl)c(=O)[nH]c1=O
Reaction #40926
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(CCCC(C)Cl)c(=O)[nH]c1=O
Reaction #40929
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #40954
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C)c(-c2cn(CCCCCl)c(=O)[nH]c2=O)o1
Reaction #40972
1-(4-Chloro-butyl)-5-(2,4-dimethyl-oxazol-5-yl)-1H-pyrimidine-2,4-dione
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)n1c(=O)c(I)cn(CCCCCl)c1=O
Reaction #41026
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(O)c(=O)n1CCCCCl)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46270
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCCCn2c1c1c(c(O)c2=O)C(=O)N(Cc2ccc(F)c(Cl)c2)CC1
Reaction #46308
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ClCCCCc1ccco1
Reaction #49655
compound
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
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