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Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
9 steps
Depiction
Dead-End Product
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
6 steps
Depiction
Dead-End Product
C(=C(C(=C(O)C(=O)O)O)O)([N+](=O)[O-])C(O)=O
Depiction
Upstream Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[NH+](CCO)CCO)Cl)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[NH+](CCO)CCO)Cl)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[NH+](CCO)CCO)Cl)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[NH+](CCO)CCO)Cl)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=CC=C1[N+](CCO)(CCO)[O-])N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=CC=C1[N+](CCO)(CCO)[O-])N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[N+](CCO)(CCO)[O-])Cl)N=NC2=C(C=C(C=C2Br)[N+](=O…
Environmental
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Upstream Precursor
C1=CC(=C(C=C1[N+](CCO)(CCO)[O-])Cl)N=NC2=C(C=C(C=C2Br)[N+](=O…
Abiotic
Depiction
Product
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Downstream Successor
2-Amino-3-bromo-5-nitrophenol
C1=C(C(=C(C=C1[N+](=O)[O-])Br)N)O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Downstream Successor
2-Amino-3-bromo-5-nitrophenol
C1=C(C(=C(C=C1[N+](=O)[O-])Br)N)O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Downstream Successor
N,N-Bis(2-hydroxyethyl)-p-phenylenediamine
C(CN(CCO)C1=CC=C(C=C1)N)O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Downstream Successor
N,N-Bis(2-hydroxyethyl)-p-phenylenediamine
C(CN(CCO)C1=CC=C(C=C1)N)O
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Downstream Successor
Benzenamine, 2-bromo-4-nitro-
C1=CC(=C(C=C1[N+](=O)[O-])Br)N
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Downstream Successor
Benzenamine, 2-bromo-4-nitro-
C1=CC(=C(C=C1[N+](=O)[O-])Br)N
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Environmental
Depiction
Downstream Successor
2-Bromo-6-chloro-4-nitroaniline
Nc1c(cc(cc1Br)[N+](=O)[O-])Cl
Depiction
Precursor
2-[4-[(2-bromo-6-chloro-4-nitrophenyl)diazenyl]-N-(2-hydroxyethyl)anilino]ethanol
C1=CC(=CC=C1N(CCO)CCO)N=NC2=C(C=C(C=C2Br)[N+](=O)[O-])Cl
Abiotic
Depiction
Downstream Successor
2-Bromo-6-chloro-4-nitroaniline
Nc1c(cc(cc1Br)[N+](=O)[O-])Cl
No Original Precursors

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