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Depiction
Upstream Precursor
CC[NH+](CCC#N)C1=CC(=C(C=C1)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O)C
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCO)N=NC2=C(C=C(C=C2)[N+](=O)[O-])Cl
Abiotic
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCO)N=NC2=C(C=C(C=C2)[N+](=O)[O-])Cl
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCOC(=O)C)N=NC2=C(C=C(C=C2)[N+](=O…
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCOC(=O)C)N=NC2=C(C=C(C=C2)[N+](=O…
Abiotic
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
Propanenitrile, 3-((4-(2-(2-chloro-4-nitrophenyl)diazenyl)-3-methylphenyl)amino)-
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])Cl
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCOC(=O)C)N=NC2=C(C=C(C=C2)[N+](=O…
Abiotic
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCO)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCO)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Abiotic
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)[NH+](CCC#N)CCO)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Environmental
Depiction
Product
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Depiction
Precursor
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Environmental
Depiction
Downstream Successor
2-Amino-5-Nitrophenol
c1cc(cc(c1N)O)[N+](=O)[O-]
Depiction
Precursor
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Abiotic
Depiction
Downstream Successor
2-Amino-5-Nitrophenol
c1cc(cc(c1N)O)[N+](=O)[O-]
Depiction
Precursor
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Abiotic
Depiction
Downstream Successor
6-Nitrocatecholamine
OC1=C(C=CC(=C1O)[N+](=O)[O-])N
Depiction
Precursor
3-[4-[(2-Hydroxy-4-nitrophenyl)diazenyl]-3-methylanilino]propanenitrile
CC1=C(C=CC(=C1)NCCC#N)N=NC2=C(C=C(C=C2)[N+](=O)[O-])O
Environmental
Depiction
Downstream Successor
6-Nitrocatecholamine
OC1=C(C=CC(=C1O)[N+](=O)[O-])N
No Original Precursors

No entries were found for this section with the current query and depth.

No Dead-Ends

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