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Depiction
Precursor
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
12 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Upstream Precursor
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Abiotic
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C=C2)O)Cl)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Abiotic
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C=C2)O)Cl)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Environmental
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C=C2)O)Cl)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Environmental
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C=C2)O)Cl)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Abiotic
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C(=C2)Cl)O)Cl)N=NC3=CC=C(C=C3)S(=O…
Environmental
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
Depiction
Upstream Precursor
CC1=C(C=CC(=C1)N=NC2=CC(=C(C(=C2)Cl)O)Cl)N=NC3=CC=C(C=C3)S(=O…
Abiotic
Depiction
Product
p-((4-((p-Hydroxyphenyl)azo)-o-tolyl)azo)-N,N-dimethylbenzenesulphonamide
CC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)O)N=NC3=CC=C(C=C3)S(=O)(=O)N(C)C
No Original Precursors

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