2-(4-chlorophenyl)ethanol

CC(=O)c1ccc(OCCc2ccc(Cl)cc2)cc1
Reaction #46017
1-{4-[2-(4-chlorophenyl)ethoxy]phenyl}ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc(CCOc2ncnc3ccccc23)cc1
Reaction #64116
4-[2-(4-Chlorophenyl)ethoxy]quinazoline
Ausbeute 2.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Clc1ccc(CCBr)cc1
Reaction #158238
2-(4-chlorophenyl)ethyl bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
SCCc1ccc(Cl)cc1
Reaction #176125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(CCOc2ncnc3ccccc23)cc1
Reaction #193958
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cccc2c(OCCc3ccc(Cl)cc3)ccnc12
Reaction #206027
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(Cl)c(OCCc2ccc(Cl)cc2)c1
Reaction #207457
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(CCBr)cc1
Reaction #210369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(Cl)ncnc1OCCc1ccc(Cl)cc1
Reaction #227469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)CC(OCC)c1ccc(OCCc2ccc(Cl)cc2)cc1
Reaction #301837
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(C=O)ccc1OC(C)c1ccc(Cl)cc1
Reaction #337837
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1cc(C=O)ccc1OC(C)c1ccc(Cl)cc1
Reaction #340594
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CN1CCC2(C)c3cc(C(=O)C(=O)OCCc4ccc(Cl)cc4)ccc3N(C)C12
Reaction #345330
1,2,3,3a,8,8a-hexahydro-α-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, 4 -chlorophenylethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
COc1c(Cl)ncnc1OCCc1ccc(Cl)cc1
Reaction #429691
4-[2-(4-chlorophenyl)ethoxy]-5-methoxy-6-chloropyrimidine
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CO.[NH4+].[OH-]
Reaction #466214
CH3OH NH4OH
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cc1nc(C(=O)N2Cc3cc4c(cc3C[C@H]2C(=O)N[C@@H](Cc2ccc(-c3ccnc(C)c3C)cc2)C(=O)O)OC[C@H](c2ccc(OCCc3ccc(Cl)cc3)cc2)O4)c(C)o1
Reaction #479148
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1nccc(-c2ccc(C[C@H](NC(=O)[C@@H]3Cc4cc5c(cc4CN3C(=O)N[C@H](C)c3ccccc3)O[C@@H](c3ccc(OCCc4ccc(Cl)cc4)cc3)CO5)C(=O)O)cc2)c1C
Reaction #479149
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Clc1ccc(CCBr)cc1
Reaction #554238
4-chlorophenethyl bromide
Ausbeute 54.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
Fc1cccc2c(OCCc3ccc(Cl)cc3)ccnc12
Reaction #574310
title product
Ausbeute 11.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
—
Reaction #700932
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
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