phenoxide

N#Cc1ccc(NCC(O)CO)cc1
Reaction #1125
p-(N-2,3-dihydroxypropylamino)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1ccc(OCC(=O)O)cc1
Reaction #5101
p-t-butylphenoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)OCCCCOc1ccc(C(C)(C)C)cc1
Reaction #5104
4-(p-tert-butylphenoxy)-butyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)c1cccc(C(C)C)c1N=Nc1cc(C(C)(C)C)cc(C(C)(C)C)c1O
Reaction #10702
phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(N=Nc2c(C(C)C)cccc2C(C)C)c(O)c(-c2c3ccccc3cc3ccccc23)c1
Reaction #10703
phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(Oc2cccc(C)n2)c(C=O)cc1-c1cccs1
Reaction #10847
4-methoxy-2-(6-methyl-pyridin-2-yloxy)-5-thiophen-2-yl-benzaldehyde
المردود 65.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc(Oc2ccccc2)c([N+](=O)[O-])c(NCCC2CCN(Cc3ccccc3)CC2)c1C
Reaction #11453
N-[2-(1-benzylpiperidin-4-yl)ethyl]-2,3-dimethyl-5-nitro-6-phenoxypyridin-4-amine
المردود 47.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(C(C)C)c(OCC#N)cc1I
Reaction #46949
(5-iodo-2-isopropyl-4-methoxy-phenoxy)-acetonitrile
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1c[nH]c2ccc(OCC(F)(F)F)cc12
Reaction #85593
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)Oc1ccccc1
Reaction #173713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc([Si](C)(C)CCCc2ccc(F)c(Oc3ccccc3)c2)cc1
Reaction #174747
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc(-c2cncc(CNCCCOc3ccccc3)c2)cc1
Reaction #179439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCCCC1Oc1ccccc1
Reaction #182385
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCC=CCCCCCCCC(=O)Oc1cc(C(=O)CNC(C)(C)C)ccc1OC(=O)c1cccnc1
Reaction #190415
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ncc(C(F)(F)F)cc1Oc1ccccc1
Reaction #198477
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(COc2ccccc2)c(C(=O)O)c1
Reaction #221359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)c(C#N)c(Oc2ccccc2)n1
Reaction #223082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Oc1ccc(Br)c(Br)c1Br)c1ccccc1CCl
Reaction #235511
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(Oc2ccc(C(=O)CNC(C)C)cc2OC(=O)c2ccccn2)cc1
Reaction #236687
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
[Na+]
Reaction #238142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
الصفحة 1التالي