methyl 4-hydroxy-3-nitrobenzoate

COC(=O)c1cc(I)c(O)c([N+](=O)[O-])c1
Reaction #42461
title compound
المردود 91075.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(O)c(N)c1
Reaction #173982
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(O)c([N+](=O)[O-])c1
Reaction #196000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(O)c(N)c1
Reaction #209716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(OCc2ccccc2)c([N+](=O)[O-])c1
Reaction #238269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(O)c(N)c1
Reaction #249016
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cc(I)c(O)c([N+](=O)[O-])c1
Reaction #436156
title compound
المردود 91075.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(O)c(N)c1
Reaction #437549
methyl 3-amino-4-hydroxybenzoate
المردود 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OCCN)c([N+](=O)[O-])c1
Reaction #437722
methyl 3-nitro4-(2-aminoethoxy)benzoate
المردود 38.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(OC[C@H](C)N)c([N+](=O)[O-])c1
Reaction #437742
methyl(S)-3-nitro-4-(2-amino-1-propoxy)benzoate
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)c1ccc(O)c(N)c1
Reaction #441487
methyl 3-amino-4-hydroxybenzoate
المردود 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COC(=O)c1ccc(OCCN)c([N+](=O)[O-])c1
Reaction #441660
methyl 3-nitro-4-(2-aminoethoxy)benzoate
المردود 38.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COC(=O)c1ccc(OC[C@H](C)N)c([N+](=O)[O-])c1
Reaction #441681
methyl(S)-3-nitro-4-(2-amino-1-propoxy)benzoate
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COC(=O)c1ccc(O)c(N)c1
Reaction #728442
3-amino-4-hydroxy-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=O)c1ccc(OCc2ccccc2)c([N+](=O)[O-])c1
Reaction #728467
4-Benzyloxy-3-nitro-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CCOC(=O)C(C)(C)Oc1ccc(C(=O)OC)cc1[N+](=O)[O-]
Reaction #768053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1ccc(OCC(C)C)c([N+](=O)[O-])c1
Reaction #902961
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1ccc(OCC(C)C)c([N+](=O)[O-])c1
Reaction #939040
desired compound
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
COC(=O)c1ccc(OCC(N)=O)c([N+](=O)[O-])c1
Reaction #950436
2-Carbamoylmethoxy-5-(methoxycarbonyl)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_02
COC(=O)c1cc(Br)c(O)c([N+](=O)[O-])c1
Reaction #1008794
Methyl 3-bromo-4-hydroxy-5-nitrobenzoate
المردود 95.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
الصفحة 1التالي