Search More · GCI-TPs

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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

Upstream Precursor

VEIFBFRKQIFTDG-UHFFFAOYSA-N

Tetranonyl benzene-1,2,4,5-tetracarboxylate

CCCCCCCCCOC(=O)C1=CC(=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC)C…

Abiotic

Product

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

Upstream Precursor

PKKCCGWISGYWRX-UHFFFAOYSA-N

2,4,5-Tris(nonoxycarbonyl)benzoic acid

CCCCCCCCCOC(=O)C1=CC(=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC)C(=O)O

Abiotic

Product

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

ZWRUINPWMLAQRD-UHFFFAOYSA-N

1-Nonanol

CCCCCCCCCO

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

Abiotic

Downstream Successor

ZWRUINPWMLAQRD-UHFFFAOYSA-N

1-Nonanol

CCCCCCCCCO

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

Abiotic

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

KKEYFWRCBNTPAC-UHFFFAOYSA-N

Terephthalic Acid

C(=O)(c1ccc(cc1)C(=O)O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

BCEQKAQCUWUNML-UHFFFAOYSA-N

4-Hydroxyisophthalic acid

c1cc(cc(c1O)C(O)=O)C(=O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

FBOCZYIJDQZQFE-UHFFFAOYSA-N

4,5-Dihydroxy-1,3-benzenedicarboxylic acid

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

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

BOPPPUCSDSHZEZ-UHFFFAOYSA-N

5-Hydroxybenzene-1,2,4-tricarboxylic acid

C(=O)(c1cc(c(cc1C(=O)O)C(=O)O)O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

Abiotic

Downstream Successor

BOPPPUCSDSHZEZ-UHFFFAOYSA-N

5-Hydroxybenzene-1,2,4-tricarboxylic acid

C(=O)(c1cc(c(cc1C(=O)O)C(=O)O)O)O

Precursor

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

CCCCCCCCCOC(=O)C1=CC=C(C=C1C(=O)OCCCCCCCCC)C(=O)OCCCCCCCCC

PriorBiotransformation

Downstream Successor

BFTIBFBURFWIAI-UHFFFAOYSA-N

5,6-Dihydroxybenzene-1,2,4-tricarboxylic acid

C(=O)(C1=C(C=C(C(=C1O)O)C(=O)O)C(=O)O)O

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

No Original Precursors

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