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Depiction
Upstream Precursor
HWATZEJQIXKWQS-UHFFFAOYSA-N
Flazasulfuron
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)OC
Depth 1
Depiction
Product
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O

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Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 1
Depiction
Downstream Successor
XPDWGBQVDMORPB-UHFFFAOYSA-N
Trifluoromethane
C(F)(F)F
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 2
Depiction
Downstream Successor
KXDHJXZQYSOELW-UHFFFAOYSA-N
Carbamic Acid
OC(=O)N
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 3
Depiction
Downstream Successor
DRAJWRKLRBNJRQ-UHFFFAOYSA-N
Hydroxycarbamic acid
OC(=O)NO
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 3
Depiction
Downstream Successor
JUJWROOIHBZHMG-UHFFFAOYSA-N
Pyridine
C1=CC=CN=C1
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 2
Depiction
Downstream Successor
PVNIIMVLHYAWGP-UHFFFAOYSA-N
Nicotinic Acid
c1cc(cnc1)C(=O)O
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 3
Depiction
Downstream Successor
KJLARRXJXZWUGO-UHFFFAOYSA-M
N-oxocarbamate
C(N=O)([O-])=O
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 3
Depiction
Downstream Successor
FJCFFCXMEXZEIM-UHFFFAOYSA-N
Oxiniacic Acid
c1cc(c[n+](c1)[O-])C(=O)O
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 3
Depiction
Downstream Successor
GRFNBEZIAWKNCO-UHFFFAOYSA-N
3-Hydroxypyridine
C1(=CN=CC=C1)O
Depiction
Precursor
BMXUAZSPKJIZRF-UHFFFAOYSA-N
N-[(4-Methoxy-6-oxo-1,6-dihydropyrimidin-2-yl)carbamoyl]-3-(trifluoromethyl)pyridine-2-sulfonamide
COC1=CC(=NC(=N1)NC(=O)NS(=O)(=O)C2=C(C=CC=N2)C(F)(F)F)O
Depth 2
Depiction
Downstream Successor
WDSONCXAIMMWHG-UHFFFAOYSA-L
C(=O)(NS(=O)(=O)[O-])[O-]

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No Original Precursors

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No Dead-Ends

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