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Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
12 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
12 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Upstream Precursor
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)CCl)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 1
Depiction
Product
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depiction
Upstream Precursor
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C(Cl)Cl)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 2
Depiction
Product
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 3
Depiction
Downstream Successor
Chloroacetate
[O-]C(=O)CCl
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 3
Depiction
Downstream Successor
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 3
Depiction
Downstream Successor
2-Chloro-5-hydroxyhexa-2,4-dienedioic acid
C(=CC=C(O)C(=O)O)(Cl)C(O)=O
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 2
Depiction
Downstream Successor
Chloroacetaldehyde
O=CCCl
Depiction
Precursor
2-[(E)-(2,5-Dichlorophenyl)diazenyl]-N-(6-ethoxy-1,3-benzothiazol-2-yl)-3-oxobutanamide
CCOC1=CC2=C(C=C1)N=C(S2)NC(=O)C(C(=O)C)N=NC3=C(C=CC(=C3)Cl)Cl
Depth 2
Depiction
Downstream Successor
2-Amino-6-benzothiazolol
OC1=CC2=C(C=C1)N=C(S2)N
No Original Precursors

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