Busqueda de Subestructura

O=C(O)Cc1ccccc1Nc1c(Cl)cccc1Cl

O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(-c2cc(=S)ss2)cc1
Reaction #46903
[2-(2,6-dichloro-phenylamino)-phenyl]-acetic acid 4-(5-thioxo-5H-[1,2]dithiol-3-yl)-phenyl ester
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #46904
4-carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #46905
compound 6
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(N=C=S)cc1
Reaction #46914
4-isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate
Rendimiento 23.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(-c2cc(=S)ss2)cc1
Reaction #72438
[2-(2,6-dichloro-phenylamino)-phenyl]-acetic acid 4-(5-thioxo-5H-[1,2]dithiol-3-yl)-phenyl ester
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #72439
4-carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #72440
compound 6
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc(N=C=S)cc1
Reaction #72448
4-isothiocyanatophenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate
Rendimiento 23.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)Oc1ccc([N+](=O)[O-])cc1
Reaction #74728
[o-(2,6-dichloroanilino)-phenyl]-acetic acid-p-nitrophenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95974
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95975
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCN(Cc1cc(C(=O)NCCCOC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc(Br)c1N)C1CCCCC1
Reaction #180849
DOI: 10.1039/C8SC04228D
Nc1c(Br)cc(C(=O)OCCCCCOC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1CN1CCCCC1
Reaction #183969
DOI: 10.1039/C8SC04228D
Nc1c(Br)cc(C(=O)OCCCCCOC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1CNC1CCCCC1
Reaction #224140
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #230165
DOI: 10.1039/C8SC04228D
CCN(Cc1cc(C(=O)OCCN(C)CCOC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc(Br)c1N)C1CCCCC1
Reaction #230493
DOI: 10.1039/C8SC04228D
COC(=O)C(O)c1ccccc1Nc1c(Cl)cccc1Cl
Reaction #237292
DOI: 10.1039/C8SC04228D
CCN(Cc1cc(C(=O)OCCCCOC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc(Br)c1N)C1CCCCCC1
Reaction #237954
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1Nc1c(Cl)cccc1Cl)OC1OC(=O)c2ccccc21
Reaction #242230
DOI: 10.1039/C8SC04228D
O=C(O)Cc1ccccc1N(Cc1ccccc1)c1c(Cl)cccc1Cl
Reaction #249744
DOI: 10.1039/C8SC04228D
Página 1Siguiente