3-phenoxybenzyl alcohol

O=Cc1cccc(Oc2ccccc2)c1
Reaction #976
aldehyde
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1cccc(Oc2ccccc2)c1
Reaction #81839
aldehyde
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
ClCc1cccc(Oc2ccccc2)c1
Reaction #165056
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
BrCc1cccc(Oc2ccccc2)c1
Reaction #177012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(C=Cc1cccc(F)c1)C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #194233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1cc(Oc2ccccc2)ccc1Br
Reaction #198453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(Nc1ccc(Cl)cc1)C(=N)OCc1cccc(Oc2ccccc2)c1
Reaction #214162
3-phenoxybenzyl 2-(4-chlorophenylamino)-3-methylbutanimidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC(C)C(C(=N)OCc1cccc(Oc2ccccc2)c1)c1ccc(Cl)cc1
Reaction #214165
3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC1(C)C(Oc2ccc(Cl)cc2)C1C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #244242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
ClCc1cccc(Oc2ccccc2)c1
Reaction #284823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cccc(Oc2ccccc2)c1
Reaction #287128
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #294811
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCc1cccc(Oc2ccccc2)c1)C12CC3CC(CC(C3)C1)C2
Reaction #301899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(F)=CC1C(C(=O)OCc2cccc(Oc3ccccc3)c2)C1(C)C
Reaction #380548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)/C=C/c1ccccc1OCc1cccc(Oc2ccccc2)c1
Reaction #409205
desired material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=Cc1cccc(Oc2ccccc2)c1
Reaction #445295
3-phenoxy-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
CC1(C)[C@H](C(=O)OCc2cccc(Oc3ccccc3)c2)[C@@H]1C=C(Br)Br
Reaction #445297
3-phenoxybenzyl(1R)cis-2,2-dimethyl-3-(2,2-dibromovinyl)-cyclopropane carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
C=CC(C)(C)CC(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #446345
3-phenoxybenzyl 3,3-dimethyl-4-pentenoate
Ausbeute 83.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
ClC(Cl)=CCOc1cc(Cl)c(Cc2cccc(Oc3ccccc3)c2)c(Cl)c1
Reaction #450241
3,5-dichloro-4-(3-phenoxybenzyl)-1-(3,3-dichloro-2-propenyloxy)-benzene
Ausbeute 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
O=C(OCc1cccc(Oc2ccccc2)c1)C12CC3CC(CC(C3)C1)C2
Reaction #458245
oily material
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
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