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Depiction
Precursor
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-chloro-2-methylphenyl)-2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC(=C2)Cl)C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-chloro-2-methylphenyl)-2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC(=C2)Cl)C)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-chloro-2-methylphenyl)-2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC(=C2)Cl)C)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(5-chloro-2-methylphenyl)-2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxobutanamide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC(=C2)Cl)C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(4-chloro-o-tolyl)-2-[(4-methyl-2-nitrophenyl)azo]-3-oxobutyramide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=C(C=C2)Cl)C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(4-chloro-o-tolyl)-2-[(4-methyl-2-nitrophenyl)azo]-3-oxobutyramide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=C(C=C2)Cl)C)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(4-chloro-o-tolyl)-2-[(4-methyl-2-nitrophenyl)azo]-3-oxobutyramide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=C(C=C2)Cl)C)[N+](=O)[O-]
Environmental
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
N-(4-chloro-o-tolyl)-2-[(4-methyl-2-nitrophenyl)azo]-3-oxobutyramide
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=C(C=C2)Cl)C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Upstream Precursor
CC1=CC(=C(C=C1)N=NC(C(=O)CCl)C(=O)NC2=CC=CC=C2C)[N+](=O)[O-]
Abiotic
Depiction
Product
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Depiction
Precursor
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Abiotic
Depiction
Downstream Successor
4-Amino-3-methylpyrocatechol
C1(=C(C(=CC=C1O)N)C)O
Depiction
Precursor
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
4-Amino-3-methylpyrocatechol
C1(=C(C(=CC=C1O)N)C)O
Depiction
Precursor
Butanamide, 2-[(4-methyl-2-nitrophenyl)azo]-N-(2-methylphenyl)-3-oxo-
CC1=CC(=C(C=C1)N=NC(C(=O)C)C(=O)NC2=C(C=CC=C2)C)[N+](=O)[O-]
Environmental
Depiction
Downstream Successor
5-Chloro-3-methyl-1,2-benzenediol
OC1=CC(=CC(=C1O)C)Cl
No Original Precursors

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