Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
3-[2-(2,4-Diamino-5-chlorophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=C(C=C(C(=C1N=NC2=CC(=C(C=C2N)N)Cl)O)S(=O)(=O)O)[N+](=O)[O-]
Abiotic
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
3-[2-(2,4-Diamino-5-chlorophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=C(C=C(C(=C1N=NC2=CC(=C(C=C2N)N)Cl)O)S(=O)(=O)O)[N+](=O)[O-]
Environmental
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
3-[2-(2,4-Diamino-5-chlorophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=C(C=C(C(=C1N=NC2=CC(=C(C=C2N)N)Cl)O)S(=O)(=O)O)[N+](=O)[O-]
Abiotic
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
3-[2-(2,4-Diamino-5-chlorophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=C(C=C(C(=C1N=NC2=CC(=C(C=C2N)N)Cl)O)S(=O)(=O)O)[N+](=O)[O-]
Environmental
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
C1=CC(=C(C=C1N)NO)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
C1=CC(=C(C=C1N)NO)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
C1=CC(=C(C=C1N)NO)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
C1=CC(=C(C=C1NO)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Upstream Precursor
C1=CC(=C(C=C1NO)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Product
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Downstream Successor
1,2,4-Benzenetriamine
c1c(c(cc(c1)N)N)N
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Downstream Successor
6-Amino-4-nitro-1-phenol-2-sulfonic acid
NC1=C(C(=CC(=C1)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Downstream Successor
6-Amino-4-nitro-1-phenol-2-sulfonic acid
NC1=C(C(=CC(=C1)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Downstream Successor
6-Amino-4-nitro-1-phenol-2-sulfonic acid
NC1=C(C(=CC(=C1)[N+](=O)[O-])S(=O)(=O)O)O
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Abiotic
Depiction
Downstream Successor
2,3,6-Triaminophenol
C1=CC(=C(C(=C1N)O)N)N
Depiction
Precursor
3-[(2,4-Diaminophenyl)diazenyl]-2-hydroxy-5-nitrobenzenesulfonic acid
C1=CC(=C(C=C1N)N)N=NC2=C(C(=CC(=C2)[N+](=O)[O-])S(=O)(=O)O)O
Environmental
Depiction
Downstream Successor
2,3,6-Triaminophenol
C1=CC(=C(C(=C1N)O)N)N
No Original Precursors

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

Search with another depth
or Explore another compound
Higher depth reveals distant relationships but increases loading time.