#794504

FC(F)(F)c1ccc(Sc2ccc(Cl)cc2)c(Br)c1
Reaction #43470
1-bromo-2-(4-chloro-phenylsulfanyl)-5-(trifluoromethyl)-benzene
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Br)c(Sc2ccc(Cl)cc2)c1
Reaction #43473
1-Bromo-2-(4-chloro-phenylsulfanyl)-4-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc(Sc2ccccc2Br)cc1
Reaction #43480
1-Bromo-2-(4-chloro-phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(Cl)cc2)c(Br)c1
Reaction #43482
1-Bromo-2-(4-chloro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(Sc2ccc(Cl)cc2)c(Br)c1
Reaction #43486
1-Bromo-2-(4-chloro-phenylsulfanyl)-5-methyl-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54049
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc(C)nc(NCSc2ccc(Cl)cc2)n1
Reaction #63140
2-[(4-chlorophenylthio)methylamino]-4-methoxy-6-methylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)C(Sc1ccc(Cl)cc1)c1ccc(Oc2ccc(Cl)cc2)cc1
Reaction #173010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1oc(=O)oc1CSc1ccc(Cl)cc1
Reaction #188512
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCCCCSc1ccc(Cl)cc1
Reaction #189024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1coc(Sc2ccc(Cl)cc2)c1
Reaction #189353
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
ClCC1(CSc2ccc(Cl)cc2)CO1
Reaction #190598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)Oc2ccc(C#N)cc2C(Sc2ccc(Cl)cc2)C1O
Reaction #199306
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(SCCCCCCCBr)cc1
Reaction #204021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)Cc1ccc(Sc2ccc(Cl)cc2)cc1
Reaction #204978
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCSc1ccc(Cl)cc1
Reaction #209773
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)C(Sc1ccc(Cl)cc1)c1ccccc1
Reaction #210160
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CCNC(=O)CSc1ccc(Cl)cc1
Reaction #213310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(c2ccccc2Sc2ccc(Cl)cc2)CCN1
Reaction #213497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CSc1ccc(Cl)cc1
Reaction #213839
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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