8-chlorooctan-1-ol

OCCCCCCCCI
Reaction #49713
8-iodooctan-1-ol
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
N#Cc1ccc(-c2ccc(OCCCCCCCCO)cc2)cc1
Reaction #237224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OCCCCCCCCCl)C1CCCO1
Reaction #256038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCCCCCCCNCCc1ccccc1
Reaction #396225
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN(CCCCCCCCO)Cc1ccccc1
Reaction #438004
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
OCCCCCCCCOc1ccccc1-c1ccccc1
Reaction #476184
8-(biphenyl-2-yloxy)-octan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(OCCCCCCCCCl)C1CCCO1
Reaction #511492
8-chlorooctyl tetrahydro-2-furancarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1ccc(S(=O)(=O)OCCCCCCCCCl)cc1
Reaction #572481
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
OCCCCCCCCOc1ccc2ccccc2c1
Reaction #572486
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
Cc1ccc(S(=O)(=O)OCCCCCCCCCl)cc1
Reaction #763021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=Cc1ccc(-c2ncc(OCCCCCCCCO)cn2)cc1
Reaction #775851
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CN(CCCCCCCCO)Cc1ccccc1
Reaction #985354
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CN(CCCCCCCCO)Cc1ccccc1
Reaction #985359
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
OCCCCCCCCOc1ccc2ccccc2c1
Reaction #1313445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
C=COCCCCCCCCCl
Reaction #1323780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CN(CCCCCCCCO)Cc1ccccc1
Reaction #1521829
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
Oc1ccc(-c2ccc(OCCCCCCCCCl)cc2)cc1
Reaction #1669078
4′-[(8-chlorooctyl)oxy]-4-biphenylol
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_05
OCCCCCCCCOc1ccccc1-c1ccccc1
Reaction #1707538
8-(biphenyl-2-yloxy)-octan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
COC(=O)/C=C/c1ccc(OCCCCCCCCCl)c(OC)c1
Reaction #1813712
methyl(2E)-3-{4-[(8-chloroctyl)oxy]-3-methoxyphenyl}-2-propenoate
Rendement 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
COC(=O)/C=C/c1ccc(OCCCCCCCCCl)c(OC)c1
Reaction #1884519
methyl (2E)-3-{4-[(8-chloroctyl)oxy]-3-methoxyphenyl}-2-propenoate
Rendement 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
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