Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

3 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

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

Upstream Precursor

XONNZQRHMVHLNV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 7-[(3-aminobenzoyl)amino]-4-hydroxy-

C1=CC(=CC(=C1)N)C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

PUVSAECARXNYFI-UHFFFAOYSA-N

C1=CC(=CC(=C1)NO)C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

WKBUUDMANLAXAT-UHFFFAOYSA-N

C1=CC(=CC(=C1)NO)C(=O)NC2=CC3=CC(=C(C(=C3C=C2)O)Cl)S(=O)(=O)O

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

WKBUUDMANLAXAT-UHFFFAOYSA-N

C1=CC(=CC(=C1)NO)C(=O)NC2=CC3=CC(=C(C(=C3C=C2)O)Cl)S(=O)(=O)O

Environmental

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

PUVSAECARXNYFI-UHFFFAOYSA-N

C1=CC(=CC(=C1)NO)C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

PUVSAECARXNYFI-UHFFFAOYSA-N

C1=CC(=CC(=C1)NO)C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

RXGHFAPOSKPIBX-UHFFFAOYSA-N

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=C(C(=C(C(=C3C=C2)O)Cl…

Abiotic

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

RXGHFAPOSKPIBX-UHFFFAOYSA-N

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=C(C(=C(C(=C3C=C2)O)Cl…

Environmental

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Upstream Precursor

QFBVBXIJMRPCEE-UHFFFAOYSA-N

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=C(C(=C3C=C2)O)Cl)…

Environmental

Product

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

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

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

C1=CC(=C(C(=C1)C(O)=O)O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

C1=CC(=C(C(=C1)C(O)=O)O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Downstream Successor

BUTHMSUEBYPMKJ-UHFFFAOYSA-N

3-Sulfopyruvic acid

C(C(O)=O)(CS(=O)(=O)O)=O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Downstream Successor

IJFXRHURBJZNAO-UHFFFAOYSA-N

3-Hydroxybenzoic Acid

OC1=CC(=CC=C1)C(=O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Downstream Successor

IJFXRHURBJZNAO-UHFFFAOYSA-N

3-Hydroxybenzoic Acid

OC1=CC(=CC=C1)C(=O)O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

C(=O)(C1=CC=CC(=C1)[N+](=O)[O-])O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

C(=O)(C1=CC=CC(=C1)[N+](=O)[O-])O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Abiotic

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

C(=O)(C1=CC=CC(=C1)[N+](=O)[O-])O

Precursor

KHRQOWDLOIPDEV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 4-hydroxy-7-((3-nitrobenzoyl)amino)-

C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC3=CC(=CC(=C3C=C2)O)S(=O)(=O)O

Environmental

Downstream Successor

HDPSONAKHMNQPA-UHFFFAOYSA-N

3,4-Dihydroxy-5-nitrobenzoic acid

OC(=O)C1=CC(=C(C(=C1)[N+](=O)[O-])O)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.

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