2-methyl-3-nitrophenol

Cc1c(N)cccc1O
Reaction #246560
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1c(N)cccc1O
Reaction #296799
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)Oc1cccc2[nH]ccc12
Reaction #344794
4-acetoxyindole
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
Cc1c(OCCCl)cccc1[N+](=O)[O-]
Reaction #450186
light yellow solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
Cc1c(OCCN(C)C)cccc1[N+](=O)[O-]
Reaction #506504
dimethyl{2-[(2-methyl-3-nitrophenyl)oxy]ethyl}amine
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1c(OC(C)(C)C)cccc1[N+](=O)[O-]
Reaction #635136
2-methyl-3-tert-butoxynitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
Cc1c(OC(C)(C)C)cccc1[N+](=O)[O-]
Reaction #650051
2-methyl-3-tert-butoxynitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1c(O)ccc(Cl)c1[N+](=O)[O-]
Reaction #705396
crude material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
Cc1c(N)cccc1O
Reaction #705400
2-methyl-3-aminophenol
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
Cc1c(OC(C)(C)C)cccc1[N+](=O)[O-]
Reaction #818698
2-methyl-3-tert-butoxynitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CC(=O)c1ccc([N+](=O)[O-])c(C)c1O
Reaction #886413
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1c(OCc2ccccc2)cccc1[N+](=O)[O-]
Reaction #903182
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)C(C)(C)Oc1cccc([N+](=O)[O-])c1C
Reaction #964356
Methyl 2-methyl-2-(2-methyl-3-nitrophenoxy)propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COc1cccc([N+](=O)[O-])c1C
Reaction #1110728
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
CCOc1cccc([N+](=O)[O-])c1C
Reaction #1135812
1-ethoxy-2-methyl-3-nitrobenzene
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
Cc1c(N)cccc1OCCN1CCCC1
Reaction #1150965
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
Cc1c(N)cccc1O
Reaction #1193906
2-methyl-3-aminophenol
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_05
CC(=O)c1ccc([N+](=O)[O-])c(C)c1O
Reaction #1248219
title compound
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCOC(=O)C(CC)Oc1cccc([N+](=O)[O-])c1C
Reaction #1335460
title compound
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_06
CC(=O)Nc1cccc(OC(C)=O)c1C
Reaction #1356960
3-(acetylamino)-2-methylphenyl acetate
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_04
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