Busqueda de Subestructura

C1CCC(C(C1)O)Cl

ClC1(Cl)CCC2OC2(Cl)C1
Reaction #50099
epoxide
DOI: 10.6084/m9.figshare.5104873.v1
OC1(O)C(F)(Cl)CCCC1(Cl)Cl
Reaction #50100
diol
Rendimiento 73.9%DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Cl
Reaction #50101
alcohol
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Cl)C1
Reaction #50102
liquid
DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(F)Cl
Reaction #50103
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(F)C1
Reaction #50104
epoxide
DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(F)Cl
Reaction #50105
alcohol
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Br
Reaction #50106
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Br)C1
Reaction #50107
epoxide
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50108
epoxide
Rendimiento 95.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50109
epoxide
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C(Cl)(Cl)CCC2OC21Cl
Reaction #50110
epoxide
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1Cl
Reaction #50111
phenol
Rendimiento 89.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1c(O)cccc1Cl
Reaction #50112
phenol
Rendimiento 75.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1c(O)cccc1Cl
Reaction #50113
phenol
Rendimiento 88.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1F
Reaction #50114
phenol
Rendimiento 21.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(Cl)C(=O)CCCC1(Cl)Cl
Reaction #50115
2-allyl-2,3,3,trichlorocyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OCC(=O)[C@@]1(OC(=O)CC)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](O)C[C@@]21C.CCCCCC
Reaction #56383
beclomethasone dipropionate n-hexane
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OCC(=O)[C@@]1(OC(=O)CC)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(Cl)[C@@H](O)C[C@@]21C.CCCCCC
Reaction #56384
beclomethasone dipropionate n-hexane
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)O[C@@H]1CCCC[C@H]1Cl)C(=O)NCCc1ccccc1
Reaction #83120
title compound
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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