Search More · GCI-TPs

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

5 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

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.

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

DLKZGMNZEDNHKO-UHFFFAOYSA-N

3-Hydroxyhexa-2,4-dienedioic acid

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

Abiotic

Downstream Successor

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Hydroquinone

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Hydroquinone

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

ZSIAUFGUXNUGDI-UHFFFAOYSA-N

1-Hexanol

OCCCCCC

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

Abiotic

Downstream Successor

ZSIAUFGUXNUGDI-UHFFFAOYSA-N

1-Hexanol

OCCCCCC

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

GGNQRNBDZQJCCN-UHFFFAOYSA-N

1,2,4-Benzenetriol

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

Precursor

CDLNMRPGGPTJLP-UHFFFAOYSA-N

4-{[4-(Hexyloxy)benzoyl]oxy}phenyl 4-(hexyloxy)benzoate

CCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCC

PriorBiotransformation

Downstream Successor

JARKCYVAAOWBJS-UHFFFAOYSA-N

Hexanal

C(CCC)CC=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.

No All Precursors

No entries were found for this section with the current query and depth.

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