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Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
15 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
15 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
10 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
Dimethylaminium
C[NH2+]C
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
Cyanoacetaldehyde
C(C#N)C=O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Abiotic
Depiction
Downstream Successor
Trimethylammonium
[NH+](C)(C)C
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
Trimethylammonium
[NH+](C)(C)C
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Abiotic
Depiction
Downstream Successor
Trimethylammonium
[NH+](C)(C)C
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
Trimethylammonium
[NH+](C)(C)C
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
3-Oxopropanoic acid
OC(=O)CC=O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Environmental
Depiction
Downstream Successor
Malonamaldehyde
C(C=O)C(N)=O
Depiction
Precursor
[2-[4-[[3-Chloro-4-(2-cyanoethylamino)phenyl]diazenyl]phenyl]-2-oxoethyl]-trimethylazanium
C[N+](C)(C)CC(=O)C1=CC=C(C=C1)N=NC2=CC(=C(C=C2)NCCC#N)Cl
Abiotic
Depiction
Downstream Successor
Malonamaldehyde
C(C=O)C(N)=O
No Original Precursors

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No All Precursors

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