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Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
10 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
10 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
6 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Upstream Precursor
CC(C(C(=O)NC1=CC=CC=C1)N=NC2=C(C=CC(=C2)S(=O)(=O)[O-])O)=O
Abiotic
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Abiotic
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Environmental
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
S(=O)(=O)(C1=CC(=C(C(=C1)Cl)O)N=NC(=C(C)O)C(=O)NC2=CC=CC=C2)O
Environmental
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
Butanamide, 2-[2-[2-hydroxy-5-[(methylamino)sulfonyl]phenyl]diazenyl]-3-oxo-N-phenyl-
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C=CC(=C2)S(=O)(=O)NC)O
Environmental
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
Butanamide, 2-[2-[2-hydroxy-5-[(methylamino)sulfonyl]phenyl]diazenyl]-3-oxo-N-phenyl-
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C=CC(=C2)S(=O)(=O)NC)O
Abiotic
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
CC(C(C(=O)NC1=CC=CC=C1Cl)N=NC2=C(C=CC(=C2)S(=O)(=O)[O-])O)=O
Abiotic
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
CC(C(C(=O)NC1=CC=CC=C1Cl)N=NC2=C(C=CC(=C2)S(=O)(=O)[O-])O)=O
Environmental
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C=CC(=C2)S(=O)(=O)N(C)O)O
Environmental
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Upstream Precursor
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C=CC(=C2)S(=O)(=O)N(C)O)O
Abiotic
Depiction
Product
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Environmental
Depiction
Downstream Successor
2-Aminophenol
C1=CC(=C(C=C1)O)N
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Abiotic
Depiction
Downstream Successor
2-Aminophenol
C1=CC(=C(C=C1)O)N
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Abiotic
Depiction
Downstream Successor
N-Phenylhydroxylamine
N(C1=CC=CC=C1)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Environmental
Depiction
Downstream Successor
N-Phenylhydroxylamine
N(C1=CC=CC=C1)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Environmental
Depiction
Downstream Successor
3-Chlorocatechol
C1(=C(C=CC=C1O)Cl)O
Depiction
Precursor
3-[(1-Anilino-1,3-dioxobutan-2-yl)diazenyl]-5-chloro-4-hydroxybenzenesulfonic acid
CC(=O)C(C(=O)NC1=CC=CC=C1)N=NC2=C(C(=CC(=C2)S(=O)(=O)O)Cl)O
Environmental
Depiction
Downstream Successor
Hydroxyquinone
OC=1C(C=CC(C1)=O)=O
No Original Precursors

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