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Depiction
Upstream Precursor
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
NCEXYHBECQHGNR-UHFFFAOYSA-N
Sulfasalazine
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
NCEXYHBECQHGNR-UHFFFAOYSA-N
Sulfasalazine
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O
Environmental
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
NCEXYHBECQHGNR-UHFFFAOYSA-N
Sulfasalazine
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
NCEXYHBECQHGNR-UHFFFAOYSA-N
Sulfasalazine
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O
Environmental
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
NCEXYHBECQHGNR-UHFFFAOYSA-N
Sulfasalazine
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC(=C(C=C3)O)C(=O)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
XNYCWWRRJOIVBY-UHFFFAOYSA-N
4-[(3-chloro-4-hydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)Cl)O
Environmental
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
XNYCWWRRJOIVBY-UHFFFAOYSA-N
4-[(3-chloro-4-hydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)Cl)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
XNYCWWRRJOIVBY-UHFFFAOYSA-N
4-[(3-chloro-4-hydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)Cl)O
Abiotic
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Depiction
Upstream Precursor
XNYCWWRRJOIVBY-UHFFFAOYSA-N
4-[(3-chloro-4-hydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)Cl)O
Environmental
Depiction
Product
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O

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Depiction
Precursor
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Abiotic
Depiction
Downstream Successor
FKESDKSQWWSINZ-UHFFFAOYSA-N
4-(Hydroxyamino)benzene-1,2-diol
c1(ccc(cc1O)NO)O
Depiction
Precursor
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Environmental
Depiction
Downstream Successor
FKESDKSQWWSINZ-UHFFFAOYSA-N
4-(Hydroxyamino)benzene-1,2-diol
c1(ccc(cc1O)NO)O
Depiction
Precursor
CBORMFPBQPCDNJ-UHFFFAOYSA-N
4-[(3,4-dihydroxyphenyl)diazenyl]-N-pyridin-2-ylbenzenesulfonamide
C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N=NC3=CC=C(C(=C3)O)O
Abiotic
Depiction
Downstream Successor
JCBGQXJYLAAINC-UHFFFAOYSA-N
Pyridin-2-ylsulfamic acid
S(=O)(=O)(NC1=CC=CC=N1)O

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

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

No Dead-Ends

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

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