2-fluoronitrobenzene

CC(C)(C)OC(=O)N[C@@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #1283
N-[(1,1-Dimethylethoxy)carbonyl]-O-(2-nitrophenyl)-L-serine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H](Oc1ccccc1[N+](=O)[O-])[C@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #1286
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #1417
N-[(1,1-Dimethylethoxy)carbonyl]-O-(2-nitrophenyl)-L-serine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H](Oc1ccccc1[N+](=O)[O-])[C@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #1420
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4118
product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #4122
N-[2-(6-methyl-1-phenyl)-1,2,3,4-tetrahydroquinolin-1-yl]-4-methyl-1-piperazine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #4126
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4176
product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #4180
N-[2-(6-methyl-1-phenyl)-1,2,3,4-tetrahydroquinolin-1-yl]-4-methyl-1-piperazine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccccc1N1CCCc2ccccc21
Reaction #4184
product
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CSCCOc1ccccc1[N+](=O)[O-]
Reaction #4337
2-(2-methylthioethoxy)-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#Cc1cccc(Oc2ccccc2[N+](=O)[O-])c1
Reaction #40425
3-(2-nitrophenoxy)benzonitrile
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1cccc(Oc2ccccc2[N+](=O)[O-])c1
Reaction #40453
3-(2-nitrophenoxy)benzonitrile
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CCN(c2ccccc2[N+](=O)[O-])c2ccccc21
Reaction #40660
1c
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CN(c2ccccc2[N+](=O)[O-])c2ccccc21
Reaction #40666
2d
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc2cccc(F)c2[nH]1
Reaction #46780
expected compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccccc1Nc1ccc(I)cc1
Reaction #50769
N-(4-iodophenyl)-2-nitroaniline
Ausbeute 48.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=[N+]([O-])c1ccccc1Nc1ccc(Oc2ccc(C(c3ccc(Oc4ccc(Nc5ccccc5[N+](=O)[O-])cc4)cc3)(C(F)(F)F)C(F)(F)F)cc2)cc1
Reaction #52251
2,2-bis[N-(2-nitrophenyl)-{4-(4-aminophenoxy)phenyl}]hexafluoropropane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)NC1CCN(c2ccccc2[N+](=O)[O-])CC1
Reaction #61157
title compound
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=[N+]([O-])c1ccccc1OC(CCl)CCl
Reaction #61384
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Seite 1Weiter