Search More · GCI-TPs

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

CCCCCCCCCOC(=O)C1=CC(=CC=C1)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

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

CCCCCCCCCOC(=O)C1=CC(=CC=C1)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

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

7 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

ROPPTGKKZZDFJN-UHFFFAOYSA-N

Trinonyl benzene-1,2,4-tricarboxylate

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

Abiotic

Product

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Upstream Precursor

BCOSAMIMJZUBFU-UHFFFAOYSA-N

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

Abiotic

Product

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

CCCCCCCCCOC(=O)C1=CC(=CC=C1)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

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Upstream Precursor

MPISGUXQHSUISV-UHFFFAOYSA-N

4,6-Bis(nonoxycarbonyl)benzene-1,3-dicarboxylic acid

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

Abiotic

Product

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Previewing top 4 entries. If you want the full results, please use the download button above.

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

YQUVCSBJEUQKSH-UHFFFAOYSA-N

Protocatechuic Acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

IJFXRHURBJZNAO-UHFFFAOYSA-N

3-Hydroxybenzoic Acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Abiotic

Downstream Successor

ZWRUINPWMLAQRD-UHFFFAOYSA-N

1-Nonanol

CCCCCCCCCO

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Abiotic

Downstream Successor

ZWRUINPWMLAQRD-UHFFFAOYSA-N

1-Nonanol

CCCCCCCCCO

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

ZWRUINPWMLAQRD-UHFFFAOYSA-N

1-Nonanol

CCCCCCCCCO

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Abiotic

Downstream Successor

BCEQKAQCUWUNML-UHFFFAOYSA-N

4-Hydroxyisophthalic acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

PriorBiotransformation

Downstream Successor

BCEQKAQCUWUNML-UHFFFAOYSA-N

4-Hydroxyisophthalic acid

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

Precursor

BSAROWVOYXDGFG-UHFFFAOYSA-N

Dinonyl benzene-1,3-dicarboxylate

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

Abiotic

Downstream Successor

QQVIHTHCMHWDBS-UHFFFAOYSA-N

Isophthalic Acid

c1cc(cc(c1)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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