4-nitrobenzoic acid

COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2517
title compound
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2518
title compound
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(OC)c(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2519
title compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c(OC)c1
Reaction #2521
title compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #2522
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1cccc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2523
title compound
Ausbeute 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccccc1C(F)(F)F)c1ccc([N+](=O)[O-])cc1
Reaction #2524
title compound
Ausbeute 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1cccc(C(F)(F)F)c1)c1ccc([N+](=O)[O-])cc1
Reaction #2525
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1cccnc1)c1ccc([N+](=O)[O-])cc1
Reaction #2526
title compound
Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1cccc([N+](=O)[O-])c1)c1ccc([N+](=O)[O-])cc1
Reaction #2528
title compound
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2529
title compound
Ausbeute 72.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #2533
title compound
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(F)cc1)c1ccc([N+](=O)[O-])cc1
Reaction #2534
title compound
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2)cc1C
Reaction #2539
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(NC(=O)c2ccc([N+](=O)[O-])cc2)c1
Reaction #2540
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(Cl)cc1)c1ccc([N+](=O)[O-])cc1
Reaction #2541
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc([N+](=O)[O-])cc1
Reaction #9849
4-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(c1ccc([N+](=O)[O-])cc1)N1CCCCC1
Reaction #11618
1-(4-nitrobenzoyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44602
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44633
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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