An 231 Reaktionen beteiligt

16083

CCOC(=O)COc1ccccc1Cl
Reaction #11412
Ethyl 2-chlorophenoxyacetate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)c1ccc(Oc2cc(N)c(N)cc2Oc2ccccc2Cl)cn1
Reaction #41577
4-(2-chlorophenoxy)-5-(6-methanesulfonyl-pyridin-3-yloxy)-benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CCCOc1ccccc1Cl
Reaction #42876
title compound
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cncc(Oc2ccccc2Cl)n1
Reaction #44557
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)COc1ccccc1Cl
Reaction #47106
product 465
Ausbeute 97.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C=C(\C)Oc1ccccc1Cl
Reaction #47273
(E)-3-(2-chloro-phenoxy)-but-2-enoic acid ethyl ester
Ausbeute 104.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Oc1c(Cl)cccc1Br
Reaction #56077
2-bromo-6-chlorophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Clc1ccccc1OCCCc1ccc(Br)cc1
Reaction #61307
3-(4Bromophenyl)prop-1-yl 2-chlorophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OC(CCCl)COc1ccccc1Cl
Reaction #92966
4-Chloro-1-(2-chlorophenoxy)-2-butanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCC(=O)Oc1ccccc1Cl
Reaction #96137
o-chlorophenyl propionate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCC(=O)Oc1ccccc1Cl
Reaction #96141
o-chlorophenyl propionate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCC(=O)Oc1ccccc1Cl
Reaction #96149
o-chlorophenyl propionate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCC(=O)Oc1ccccc1Cl
Reaction #96301
o-chlorophenyl propionate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cn1nc(C(F)(F)F)c(CSC2=NOC(C)(C)C2)c1Oc1ccccc1Cl
Reaction #181604
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCOc1cc(Oc2ccccc2Cl)ncn1
Reaction #186019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(Cc1cccc(OCCCOc2ccccc2Cl)c1)C(=O)O
Reaction #187986
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CCl)COc1ccccc1Cl
Reaction #193217
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1c(Cl)cc(Cl)cc1Cl
Reaction #224180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)N1C(=O)C(NCCCOc2ccccc2Cl)=C(c2ccccc2)S1(=O)=O
Reaction #230065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(Nc2cc3ccccc3c(Oc3ccccc3Cl)n2)n[nH]1
Reaction #238034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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