4-nitrobenzoyl chloride

O=C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #1435
1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc2c(c1)OCO2)c1ccc([N+](=O)[O-])cc1
Reaction #2542
title compound
Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2nccn2Cc2ccccc21
Reaction #3618
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2-c2ccccc21
Reaction #3622
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccoc21
Reaction #3629
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2ccnn2Cc2ccccc21
Reaction #3634
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccsc21
Reaction #3639
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2sccc21
Reaction #3644
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2cccn2-c2ccccc21
Reaction #3648
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2nncn2-c2ccccc21
Reaction #3655
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #5675
5-dimethylamino-1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(O)COC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #8582
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc([N+](=O)[O-])cc4)c3C2=O)C(=O)N1
Reaction #10106
N-[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-4-nitro-benzamide
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #54530
yellow needles
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #56966
solid
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H]1O[C@@H](OC(=O)c2ccc([N+](=O)[O-])cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
Reaction #58014
material
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCC(=NOCC)C1=C(OC(=O)c2ccc([N+](=O)[O-])cc2)CC(c2c(C)cc(C)c(C(C)=O)c2C)CC1=O
Reaction #64054
5-(3-acetyl-2,4,6-trimethylphenyl)-2-[1-(ethoxyimino)butyl]-3-(4-nitrobenzoyl)oxy-cyclohex-2-en-1-one
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(c1ccc(Br)cc1)c1ccc([N+](=O)[O-])cc1
Reaction #64266
yellow crystals
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NS(=O)(=O)c1ccc(Cl)s1)c1ccc([N+](=O)[O-])cc1
Reaction #66418
titled compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCCCCCCCCCOC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #68698
tetradecyl 4-nitrobenzoate
Ausbeute 47.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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