Busqueda de Subestructura

CN(C)CCCl

Cl.O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2554
title compound
Rendimiento 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2555
title compound
Rendimiento 92.3%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2564
title compound
Rendimiento 54.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3928
1-(4-chlorobenzyl)-4-(2-chloroethyl)piperazine dihydrochloride
Rendimiento 112.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.SCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3929
2-[4-(4-chlorobenzyl)piperazin-1-yl]ethanethiol dihydrochloride
Rendimiento 97.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(OCCN(Cc2ccccc2)Cc2ccccc2)c1O
Reaction #4642
3-(2-dibenzylaminoethoxy)salicyclic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)ncn2CCCCN1CCN(c2ccc3c(c2)OCCO3)CC1
Reaction #5051
6-[4(4-(5-ethoxycarbonylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxane
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCl)C1CC(=O)N(Cc2ccccc2)C1=O
Reaction #64943
1-Benzyl-3-(2-chloroethyl-methyl-amino )-pyrrolidine2,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(O)CC(C)(C)N1[O].O=C(O)CCCc1ccc(N(CCCl)CCCl)cc1
Reaction #68768
Chlorambucil TEMPOL
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)CCl)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #72091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2cc(F)ccc2F)CC1
Reaction #77298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2cc(F)c(F)cc2F)CC1
Reaction #77299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1C1CCN(CCN2C(=O)CC3(CCCC3)CC2=O)CC1
Reaction #77304
title compound
Rendimiento 7.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cl)cc1N1CCN(CCN2C(=O)CC3(CCCC3)CC2=O)CC1
Reaction #77305
title compound
Rendimiento 49.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2c(F)cccc2F)CC1
Reaction #77306
title compound
Rendimiento 26.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2ccc(F)c(F)c2)CC1
Reaction #77307
title compound
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(CC)CN(CC(CC)CCCC)C(=O)C(Cl)c1ccccc1
Reaction #89797
2-chloro-N,N-bis(2-ethylhexyl)-2-phenyl-acetamide
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(Cl)CS[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)O
Reaction #94054
7-phenoxyacetoamido-3-chloro-3-methyl-cepham-4-carboxylic acid
Rendimiento 51.5%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #170241
gum
Rendimiento 109.0%DOI: 10.6084/m9.figshare.5104873.v1
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