Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
11 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Upstream Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-Chloro-2-methylphenyl)-2-[(E)-(4-chloro-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=C(C=C(C=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-Chloro-2-methylphenyl)-2-[(E)-(4-chloro-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=C(C=C(C=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-Chloro-2-methylphenyl)-2-[(E)-(4-chloro-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=C(C=C(C=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-Chloro-2-methylphenyl)-2-[(E)-(4-chloro-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=C(C=C(C=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
Butanamide, N-(4-chloro-2-methylphenyl)-2-[2-(4-chloro-2-nitrophenyl)diazenyl]-3-oxo-
CC1=C(C=CC(=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
Butanamide, N-(4-chloro-2-methylphenyl)-2-[2-(4-chloro-2-nitrophenyl)diazenyl]-3-oxo-
CC1=C(C=CC(=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
CC1=CC=CC=C1NC(=O)C(C(=O)CCl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
CC1=CC=CC=C1NC(=O)C(C(=O)CCl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Upstream Precursor
Butanamide, N-(4-chloro-2-methylphenyl)-2-[2-(4-chloro-2-nitrophenyl)diazenyl]-3-oxo-
CC1=C(C=CC(=C1)Cl)NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
3-Methylcatechol
c1(cccc(c1O)C)O
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
4-Amino-3-methylpyrocatechol
C1(=C(C(=CC=C1O)N)C)O
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Abiotic
Depiction
Downstream Successor
4-Amino-3-methylpyrocatechol
C1(=C(C(=CC=C1O)N)C)O
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
5-Chloro-3-methyl-1,2-benzenediol
OC1=CC(=CC(=C1O)C)Cl
Depiction
Precursor
Butanamide, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-N-(2-methylphenyl)-3-oxo-
CC1=CC=CC=C1NC(=O)C(C(=O)C)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
2-Amino-m-cresol
Cc1c(c(ccc1)O)N
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.