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Depiction
Precursor
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
8 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
Abiotic
Depiction
Product
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
Depiction
Upstream Precursor
CCN(CC)C1=C(C(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O)Cl
Environmental
Depiction
Product
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
Depiction
Upstream Precursor
CCN(CC)C1=C(C(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O)Cl
Environmental
Depiction
Product
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
Depiction
Upstream Precursor
CC[N+](CC)(C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O)[O-]
Abiotic
Depiction
Product
6-[2-(5-Chloropyridin-2-yl)hydrazinylidene]-3-(diethylamino)cyclohexa-2,4-dien-1-one
CCN(CC)C1=CC(=C(C=C1)N=NC2=NC=C(C=C2)Cl)O
No Original Precursors

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