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Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
12 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
12 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
7 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
Depth 1
Depiction
Downstream Successor
Trimethylammonium
[NH+](C)(C)C
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
Depth 3
Depiction
Downstream Successor
2-Aminophenol
C1=CC(=C(C=C1)O)N
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
Depth 3
Depiction
Downstream Successor
Anthranilic Acid
OC(=O)C1=C(C=CC=C1)N
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
Depth 3
Depiction
Downstream Successor
Chloroformic acid
C(O)(Cl)=O
Depiction
Precursor
2-[2-[4-[(5-Chloro-2-cyanophenyl)diazenyl]-3-methylphenyl]ethylamino]ethyl-trimethylazanium
CC1=C(C=CC(=C1)CCNCC[N+](C)(C)C)N=NC2=C(C=CC(=C2)Cl)C#N
Depth 3
Depiction
Downstream Successor
CID 417
C(C=C(C=CC(O)=O)Cl)(O)=O
No Original Precursors

No entries were found for this section with the current query and depth.

No All Precursors

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