Search More · GCI-TPs

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=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

NVMCTYFWKJPYBA-UHFFFAOYSA-N

Benzamide, N-[4,5-dihydro-5-oxo-1-(2,4,6-trichlorophenyl)-1H-pyrazol-3-yl]-3-nitro-

C1C(=NN(C1=O)C2=C(C=C(C=C2Cl)Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

NVMCTYFWKJPYBA-UHFFFAOYSA-N

Benzamide, N-[4,5-dihydro-5-oxo-1-(2,4,6-trichlorophenyl)-1H-pyrazol-3-yl]-3-nitro-

C1C(=NN(C1=O)C2=C(C=C(C=C2Cl)Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

KYMBTETYOFJZER-UHFFFAOYSA-N

C1C(=NN(C1=O)C2=C(C=C(C=C2)Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

KYMBTETYOFJZER-UHFFFAOYSA-N

C1C(=NN(C1=O)C2=C(C=C(C=C2)Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

ZSUCZFNOCZVGCA-UHFFFAOYSA-N

C1C(=NN(C1=O)C2=C(C=CC=C2Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

ZSUCZFNOCZVGCA-UHFFFAOYSA-N

C1C(=NN(C1=O)C2=C(C=CC=C2Cl)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

FGUBIYPTORTEKB-UHFFFAOYSA-N

C1C(=NN(C1=O)C2=C(C=CC=C2)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Upstream Precursor

LVJUPCSXWKDVML-UHFFFAOYSA-N

N-[1-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]-3-nitrobenzamide

C1C(=NN(C1=O)C2=CC=C(C=C2)Cl)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Product

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Previewing top 8 entries. If you want the full results, please use the download button above.

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

IJFXRHURBJZNAO-UHFFFAOYSA-N

3-Hydroxybenzoic Acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

IJFXRHURBJZNAO-UHFFFAOYSA-N

3-Hydroxybenzoic Acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

GNWREYFHYLIYJE-UHFFFAOYSA-N

3,4-Dihydroxybenzamide

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

LQNUZADURLCDLV-UHFFFAOYSA-N

Nitrobenzene

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

LQNUZADURLCDLV-UHFFFAOYSA-N

Nitrobenzene

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

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

Precursor

NNGHWPIQPQHOKQ-UHFFFAOYSA-N

Stk391643

C1C(=NN(C1=O)C2=CC=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Environmental

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

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