4-nitrophenylacetic acid

CCN(CCO)C(=CC=Cc1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #6295
4-(N-2-hydroxyethyl-N-ethylamino)-4'-nitro-1,4-diphenyl-1,3-butadiene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Oc1ccc(C=C(C(=O)O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #6511
a-p-Nitrophenyl-p-acetoxycinnamic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Oc1ccc(C=C(C(=O)O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #6516
a-p-Nitrophenyl-p-acetoxycinnamic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Cc1ccc([N+](=O)[O-])cc1)N1CCCCC1
Reaction #11648
2-(4-nitro-phenyl)-1-piperidin-1-yl-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cc1ccc([N+](=O)[O-])cc1)N1CCOCC1
Reaction #11658
1-morpholin-4-yl-2-(4-nitro-phenyl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(NC(=O)Cc1ccc([N+](=O)[O-])cc1)C(=O)OCC(C)C
Reaction #51356
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #51527
4-nitrophenylacetone
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #51528
4-nitrophenylacetone
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)c1c(N)sc(-c2ccc([N+](=O)[O-])cc2)c1C
Reaction #51529
ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate
المردود 63.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc2c(cc1OC)C(C)N(C(=O)Cc1ccc([N+](=O)[O-])cc1)CC2
Reaction #63502
N-(4-nitrophenylacetyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CC(=O)Oc1ccc(C=C(C(=O)O)c2ccc([N+](=O)[O-])cc2)cc1
Reaction #82138
α-p-Nitrophenyl-p-acetoxycinnamic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #169469
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)Cc1ccc2[nH]ccc2c1
Reaction #216698
product ( 6 )
المردود 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCC(NC(=O)Cc1ccc([N+](=O)[O-])cc1)C(=O)OCC(C)C
Reaction #220545
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1cc(C=Cc2ccc([N+](=O)[O-])cc2)cc(OC)c1OC
Reaction #222259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cc1ccc([N+](=O)[O-])cc1)N1CCOCC1
Reaction #225724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #241094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCOC(=O)NC(Cc1cc(C2CCCN2C(=O)Cc2ccc([N+](=O)[O-])cc2)no1)C(=O)OCC
Reaction #249615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #264739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC(NC(=O)Cc1ccc([N+](=O)[O-])cc1)C(=O)OCC(C)C
Reaction #265692
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي