Search More · GCI-TPs

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

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.

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

Abiotic

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

MWRVRCAFWBBXTL-UHFFFAOYSA-N

4-Hydroxyphthalic acid

C(=O)(c1c(cc(cc1)O)C(=O)O)O

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

WERYXYBDKMZEQL-UHFFFAOYSA-N

1,4-Butanediol

C(CCO)CO

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

Abiotic

Downstream Successor

WERYXYBDKMZEQL-UHFFFAOYSA-N

1,4-Butanediol

C(CCO)CO

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

QXGJCWSBOZXWOV-UHFFFAOYSA-N

3,4-Dihydroxyphthalic acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

Abiotic

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

KKEYFWRCBNTPAC-UHFFFAOYSA-N

Terephthalic Acid

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

Precursor

XOTMHFNWERTCLG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(4-(ethenyloxy)butyl) ester

C=COCCCCOC(=O)C1=CC(=C(C=C1)C(=O)OCCCCOC=C)C(=O)OCCCCOC=C

PriorBiotransformation

Downstream Successor

BCEQKAQCUWUNML-UHFFFAOYSA-N

4-Hydroxyisophthalic acid

c1cc(cc(c1O)C(O)=O)C(=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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No All Precursors

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