HNO3

CC(=O)Nc1ccc([N+](=O)[O-])c(C)c1C(=O)O
Reaction #901
2-Methyl-3-nitro-6-acetamidobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
Reaction #1479
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(=O)[nH]c(=O)n(-c2cc([N+](=O)[O-])c(F)cc2Cl)c1=O
Reaction #1561
title product
المردود 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(=O)n(CC(=O)O)c(=O)n(-c2cc([N+](=O)[O-])c(F)cc2Cl)c1=O
Reaction #1566
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1cc([N+](=O)[O-])c(Cl)cc1F
Reaction #1574
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C2=C(CCCC2)C(=O)N1c1cc([N+](=O)[O-])c(Cl)cc1F
Reaction #1581
title product
المردود 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C(=O)O)C(=O)c1ccc(Cl)c([N+](=O)[O-])c1
Reaction #1590
4-chloro-3-nitrobenzoylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1cc(OC(F)(F)F)ccc1[N+](=O)[O-]
Reaction #1838
2-Nitro-5-trifluoromethoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Cl)c(Cl)cc1[N+](=O)[O-]
Reaction #1842
4,5-Dichloro-2-nitrotoluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1cc(Cl)ccn1
Reaction #1945
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(N)Nc1cccc(C(F)(F)F)c1.O=[N+]([O-])O
Reaction #2251
3-trifluoromethyl-phenylguanidine nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C(=O)O)C(=O)c1ccc(Cl)c([N+](=O)[O-])c1
Reaction #2263
4-chloro-3-nitrobenzoylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCNc1nc2c([N+](=O)[O-])c(O)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3254
title compound
المردود 52.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCn1c(=O)c2[nH]c([N+](=O)[O-])nc2n(CCCC)c1=O
Reaction #3724
1,3-Di-n-butyl-8-nitro Xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c2[nH]c([N+](=O)[O-])nc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3725
product
المردود 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1nc(N)c([N+](=O)[O-])c(OC)n1
Reaction #4227
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(Br)c(NS(=O)(=O)c2ccccc2)cc1Br
Reaction #4328
2,5-dibromo-4-nitro-N-benzenesulphonylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(F)c(NS(=O)(=O)c2ccccc2)cc1F
Reaction #4331
2,5-difluoro-4-nitro-N-benzenesulphonylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
Reaction #4359
2,4-dichloro-5-fluoro-3-nitro-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
Reaction #4442
crude product
المردود 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
الصفحة 1التالي