Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
10 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
10 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Upstream Precursor
1-Decyl 2-((1-(2-chloro-5-sulphophenyl)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-4-yl)azo)benzoate
CCCCCCCCCCOC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O…
Abiotic
Depiction
Product
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Depiction
Upstream Precursor
1-Decyl 2-((1-(2-chloro-5-sulphophenyl)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-4-yl)azo)benzoate
CCCCCCCCCCOC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O…
PriorBiotransformation
Depiction
Product
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
C(C(O)=O)(=CC=C(C(O)=O)C(=O)O)O
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Abiotic
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=CC=CC=C2C(=O)O)C3=CC(=CC=C3)S(=O)(=O)[O-]
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=CC=CC=C2C(=O)O)C3=CC(=CC=C3)S(=O)(=O)[O-]
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Abiotic
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=CC=CC=C2C(=O)O)C3=CC(=CC(=C3O)O)S(=O)(=O)[O-]
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=CC=CC=C2C(=O)O)C3=CC(=CC(=C3O)O)S(=O)(=O)[O-]
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Abiotic
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=C(C=CC=C2)O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
CC1=NN(C(=O)C1N=NC2=CC=CC(=C2O)O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Abiotic
Depiction
Downstream Successor
C(=O)(C1=CC(=C(C=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)C…
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
C(=O)(C1=CC(=C(C=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)C…
Depiction
Precursor
2-[[1-(2-chloro-5-sulfophenyl)-3-methyl-5-oxo-4H-pyrazol-4-yl]diazenyl]benzoic acid
OC(=O)C1=CC=CC=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)Cl)C
Environmental
Depiction
Downstream Successor
C(=O)(C1=CC=C(C(=C1N=NC2C(=NN(C2=O)C3=C(C=CC(=C3)S(=O)(=O)O)C…
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.