2-chloro-5-nitro phenol

Nc1ccc(Cl)c(O)c1
Reaction #8726
2-Chloro-5-aminophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(Cl)c(OCc2ccccc2)c1
Reaction #66110
2-benzyloxy-1-chloro-4-nitro-benzene
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)=CCOc1cc([N+](=O)[O-])ccc1Cl
Reaction #78290
1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Nc1ccc(Cl)c(O)c1
Reaction #176207
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(Cl)c(OCC2CCCO2)c1
Reaction #226465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CC(COc2cc([N+](=O)[O-])ccc2Cl)C1
Reaction #230872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C)Oc1cc([N+](=O)[O-])ccc1Cl
Reaction #272615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(Cl)c(O)c1
Reaction #293887
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccc(Cl)c(OCc2ccccc2)c1
Reaction #384505
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc(Cl)c(OCCCBr)c1
Reaction #417971
title compound 26a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C=CCOc1cc([N+](=O)[O-])ccc1Cl
Reaction #431772
1-(allyloxy)-2-chloro-5-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
C=CCc1c(N2C(=O)C3=C(CCCC3)C2=O)ccc(C)c1O
Reaction #431776
N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
C=CCOc1cc([N+](=O)[O-])ccc1Cl
Reaction #561407
2-(allyloxy)-1-chloro-4-nitrobenzene
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)OC(=O)NCCCOc1cc([N+](=O)[O-])ccc1Cl
Reaction #561418
tert-butyl 3-(2-chloro-5-nitrophenoxy)propylcarbamate
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COc1ccc(COc2cc([N+](=O)[O-])ccc2Cl)cc1
Reaction #561420
1-chloro-2-(4-methoxybenzyloxy)-4-nitrobenzene
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOC(=O)C(C)Oc1cc([N+](=O)[O-])ccc1Cl
Reaction #572394
ethyl α-(2-chloro-5-nitrophenoxy)propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
CC(C)(C)OC(=O)N1CCC[C@H]1COc1cc([N+](=O)[O-])ccc1Cl
Reaction #578773
(S)-2-(2-Chloro-5-nitro-phenoxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)(C)OC(=O)N1CCC(COc2cc([N+](=O)[O-])ccc2Cl)CC1
Reaction #578782
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=[N+]([O-])c1ccc(Cl)c(OCC2CCCO2)c1
Reaction #578786
2-(2-Chloro-5-nitro-phenoxymethyl)-tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Nc1ccc(Cl)c(O)c1
Reaction #578788
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
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