Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
3 steps
Depiction
Dead-End Product
Carbonic Acid
C(=O)(O)O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
5 steps
Depiction
Dead-End Product
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
6 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
11 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
11 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
5 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Upstream Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(=O)OC)Cl)O
Environmental
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(=O)OC)Cl)O
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C(=C1)Cl)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C(=C1)Cl)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C(=C1)Cl)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(…
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C(=C1)Cl)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(…
Environmental
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(=O)OC)Cl)O
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C(=CC3=C2C(=CC=C3)NC(=O)OC)Cl)O
Environmental
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Upstream Precursor
CCNS(=O)(=O)C1=CC(=C(C(=C1)Cl)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Abiotic
Depiction
Product
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Downstream Successor
Methanol
CO
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Downstream Successor
Acetaldehyde
C(C)=O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Abiotic
Depiction
Downstream Successor
Acetaldehyde
C(C)=O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Downstream Successor
Formic Acid
OC=O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Abiotic
Depiction
Downstream Successor
Formic Acid
OC=O
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Downstream Successor
Ethylamine
NCC
Depiction
Precursor
methyl N-[8-[[5-(ethylsulfamoyl)-2-hydroxyphenyl]diazenyl]-7-hydroxynaphthalen-1-yl]carbamate
CCNS(=O)(=O)C1=CC(=C(C=C1)O)N=NC2=C(C=CC3=C2C(=CC=C3)NC(=O)OC)O
Environmental
Depiction
Downstream Successor
2-Aminophenol
C1=CC(=C(C=C1)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.