3,5-dinitrobenzoic acid

CC#C[C@@H](C[C@H](C)CCCC(C)C)OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #55270
6(R),10-Dimethyl-undecan-2-yn-4(R)-ol 3,5-dinitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #163950
3,5-Dinitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cc(CO)cc([N+](=O)[O-])c1
Reaction #163952
title compound 6
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #184329
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #197747
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)C1(c2ccccc2F)CO1
Reaction #209860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #294967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[C@H](OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)[C@@]1(c2ccccc2F)CO1
Reaction #366343
[(1S)-1-[(2R)-2-(2-fluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=C(Cl)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #467901
3,5-dinitrobenzoic chloride
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
C=CS(=O)(=O)CS(=O)(=O)C=C
Reaction #514076
bis(vinylsulfonyl)methane
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_10
C=CS(=O)(=O)CS(=O)(=O)C=C
Reaction #514077
bis(vinylsulfonyl)methane
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_10
C[C@H](OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)[C@@]1(c2ccccc2F)CO1
Reaction #569239
[(1S)-1-[(2R)-2-(2-fluorophenyl)-2-oxiranyl)ethyl] 3,5-dinitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
O=C1C=CC=C/C1=C/NCCN/C=C1\C=CC=CC1=O.[Co+3]
Reaction #586099
Cobalt-(III) Salen
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(OCCCCCCO)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #598891
6-hydroxyhexyl 3,5-dinitrobenzoate
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
O=C(OCCCCCCO)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #610520
6-hydroxyhexyl 3,5-dinitrobenzoate
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(OCCCO)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #725705
white crystals
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_12
COC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #755062
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)C1(c2ccccc2F)CO1
Reaction #770713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc(C(=O)O)cc([N+](=O)[O-])c1
Reaction #898349
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #903707
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Página 1Siguiente