2-fluoro-5-nitrotoluene

Cc1cc([N+](=O)[O-])ccc1NN.F
Reaction #1184
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc([N+](=O)[O-])ccc1NCC1CCCO1
Reaction #54617
2-methyl-4-nitro-N-tetrahydrofurfurylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Cc1cc([N+](=O)[O-])ccc1-n1cccc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c1=O
Reaction #172379
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc([N+](=O)[O-])ccc1-n1cccc(Br)c1=O
Reaction #172381
3-Bromo-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1ccc(F)c(CBr)c1
Reaction #172393
2-(Bromomethyl)-1-fluoro-4-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cccn(-c2ccc([N+](=O)[O-])cc2C)c1=O
Reaction #172402
3-Methoxy-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc([N+](=O)[O-])ccc1-n1cccc(Br)c1=O
Reaction #180476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(F)c(CBr)c1
Reaction #191074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
F
Reaction #194530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc([N+](=O)[O-])ccc1N(CCO)CCO
Reaction #198969
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc([N+](=O)[O-])ccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #206238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc([N+](=O)[O-])ccc1N1CCSCC1
Reaction #221639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc([N+](=O)[O-])ccc1NCC(O)CO
Reaction #234529
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc([N+](=O)[O-])ccc1Oc1ccccc1
Reaction #235278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc([N+](=O)[O-])ccc1NCCN(CCO)CCO
Reaction #250676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(Oc2ccc([N+](=O)[O-])cc2C)cn1
Reaction #256970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(Oc2ccc([N+](=O)[O-])cc2C)cn1
Reaction #269264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc([N+](=O)[O-])ccc1N1CCC(O)CC1
Reaction #286288
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCN(CC)CCOc1ccc([N+](=O)[O-])cc1C
Reaction #288861
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc([N+](=O)[O-])ccc1-n1cnc(C(F)(F)F)c1
Reaction #288941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي