Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Abiotic
Depiction
Product
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Depiction
Upstream Precursor
CCCCC1(C(=O)N(N(C1=O)C2=CC(=C(C(=C2)Cl)O)Cl)C3=CC=CC=C3)CO
Abiotic
Depiction
Product
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Depiction
Upstream Precursor
CCCCC1(C(=O)N(N(C1=O)C2=CC(=C(C(=C2)Cl)O)Cl)C3=CC=CC=C3)CO
Environmental
Depiction
Product
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Depiction
Upstream Precursor
CCCCC1(C(=O)N(N(C1=O)C2=CC(=C(C=C2)O)Cl)C3=CC=CC=C3)CO
Abiotic
Depiction
Product
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Depiction
Upstream Precursor
CCCCC1(C(=O)N(N(C1=O)C2=CC(=C(C=C2)O)Cl)C3=CC=CC=C3)CO
Abiotic
Depiction
Product
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Depiction
Precursor
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Abiotic
Depiction
Downstream Successor
2,3-Dihydroxyhexa-2,4-dienedioic acid
OC(=C(C=CC(=O)O)O)C(O)=O
Depiction
Precursor
4-Butyl-4-(hydroxymethyl)-1-(4-hydroxyphenyl)-2-phenylpyrazolidine-3,5-dione
CCCCC1(C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3)CO
Abiotic
Depiction
Downstream Successor
4-(2-Phenylhydrazinyl)phenol
N(NC1=CC=C(C=C1)O)C2=CC=CC=C2
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.