Substructure Search

556862

CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #76503
9-Ethyl-1,4,7,8,9,10-hexahydro-6-nitro-pyrido[3,4-f]quinoxaline-2,3-dione
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1.CS(=O)(=O)O
Reaction #76504
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #253034
DOI: 10.1039/C8SC04228D
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1193624
solid
Yield 104.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1618038
solid
Yield 104.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CC(=O)N1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #1826856
solid
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O
Reaction #2425678
DOI: 10.1039/C8SC04228D
CCN1CCc2c([N+](=O)[O-])cc3[nH]c(=O)c(=O)[nH]c3c2C1
Reaction #2433584
DOI: 10.1039/C8SC04228D