Search More · GCI-TPs

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

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

11 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

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

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

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

RCFAHSGZAAFQJH-UHFFFAOYSA-N

2,4-Bis(1-Phenylethyl)Phenol

C1(=C(C=C(C=C1)C(C)C2=CC=CC=C2)C(C)C3=CC=CC=C3)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Abiotic

Downstream Successor

RCFAHSGZAAFQJH-UHFFFAOYSA-N

2,4-Bis(1-Phenylethyl)Phenol

C1(=C(C=C(C=C1)C(C)C2=CC=CC=C2)C(C)C3=CC=CC=C3)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Abiotic

Downstream Successor

JGQFJINLNIZJKI-UHFFFAOYSA-N

CC(C1=CC=CC=C1)C(C=C(C(O)=O)C(C)C2=CC=CC=C2)=C(C(O)=O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

JGQFJINLNIZJKI-UHFFFAOYSA-N

CC(C1=CC=CC=C1)C(C=C(C(O)=O)C(C)C2=CC=CC=C2)=C(C(O)=O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

MMRDEVVSULAJOJ-UHFFFAOYSA-N

CC(c1cc(c(cc1)O)O)c2cc(c(cc2)O)C(C)c3ccccc3

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

OQHYVRHLAURZMQ-UHFFFAOYSA-N

CC(c1ccccc1)c2cc(c(cc2)O)C(C)c3cc(c(cc3)O)O

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Abiotic

Downstream Successor

MZMWBPFLMRVXAZ-UHFFFAOYSA-N

CC(C1=CC(=C(C=C1)O)C(C)C2=CC=CC=C2)C3C=CC(=O)C=C3

Precursor

UXDLAKCKZCACAX-UHFFFAOYSA-N

2-hydroxy-3,5-bis(1-phenylethyl)benzoic Acid

CC(C1=CC=CC=C1)C2=CC(=C(C(=C2)C(=O)O)O)C(C)C3=CC=CC=C3

Environmental

Downstream Successor

MZMWBPFLMRVXAZ-UHFFFAOYSA-N

CC(C1=CC(=C(C=C1)O)C(C)C2=CC=CC=C2)C3C=CC(=O)C=C3

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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