Search More · GCI-TPs

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

2 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

10 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

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Upstream Precursor

PNOPPOAENKHWKO-UHFFFAOYSA-N

1,2-Benzenedicarboxylic acid, 4,4'-(hydroxymethylene)bis-, ar,ar'-dimethyl ester

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

Environmental

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

PNOPPOAENKHWKO-UHFFFAOYSA-N

1,2-Benzenedicarboxylic acid, 4,4'-(hydroxymethylene)bis-, ar,ar'-dimethyl ester

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

Abiotic

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

BYFOQPSEUXLIOQ-UHFFFAOYSA-N

1,2-Benzenedicarboxylic acid, 4,4'-carbonylbis-, ar,ar'-diethyl ester

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

Environmental

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

BYFOQPSEUXLIOQ-UHFFFAOYSA-N

1,2-Benzenedicarboxylic acid, 4,4'-carbonylbis-, ar,ar'-diethyl ester

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

Abiotic

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

WONZPRWRROIFKA-UHFFFAOYSA-N

4-(4-Carboxy-3-ethoxycarbonylbenzoyl)phthalic acid

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

Environmental

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

WONZPRWRROIFKA-UHFFFAOYSA-N

4-(4-Carboxy-3-ethoxycarbonylbenzoyl)phthalic acid

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

Abiotic

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

RPCYLARQJOZEMG-UHFFFAOYSA-N

4-(3-Carboxy-4-methoxycarbonylbenzoyl)phthalic acid

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

Environmental

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

RPCYLARQJOZEMG-UHFFFAOYSA-N

4-(3-Carboxy-4-methoxycarbonylbenzoyl)phthalic acid

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

Abiotic

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

LRGSIYDSLBWHOE-UHFFFAOYSA-N

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

Environmental

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Upstream Precursor

LRGSIYDSLBWHOE-UHFFFAOYSA-N

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

Abiotic

Product

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

RZSHABLUYDDEES-UHFFFAOYSA-N

4-(3-Carboxybenzoyl)phthalic acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Environmental

Downstream Successor

RZSHABLUYDDEES-UHFFFAOYSA-N

4-(3-Carboxybenzoyl)phthalic acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

GQHQCHOIAADKDO-UHFFFAOYSA-N

4-(4-Carboxybenzoyl)phthalic acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Environmental

Downstream Successor

GQHQCHOIAADKDO-UHFFFAOYSA-N

4-(4-Carboxybenzoyl)phthalic acid

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

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

OLPIYKRFUKXUJH-UHFFFAOYSA-N

C1=CC(=C(C=C1C(=O)C=2C(C=C(C(C(=O)O)C2)C(=O)O)=O)C(=O)O)C(=O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

RAMQLWQLYNMGDY-UHFFFAOYSA-N

C1=CC(=C(C=C1C(=O)C2=CC(=C(C=C2)C(=O)O)C(=O)O)C(=O)O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Environmental

Downstream Successor

DMVUBOJXTRTCFC-UHFFFAOYSA-N

C1(=C(C=C(C=C1O)C(=O)C2=CC(=C(C=C2)C(=O)O)C(=O)O)C(=O)O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

IALAQFKRTOWRIU-UHFFFAOYSA-N

C1=CC(=C(C=C1C(=O)C2=CC(=C(C=C2O)C(=O)O)C(=O)O)C(=O)O)C(=O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Abiotic

Downstream Successor

FYYGWPISCVUUTL-UHFFFAOYSA-N

C1=CC(=C(C=C1C(=O)C2=CC(=C(C=C2)C(=O)O)C(=O)O)O)C(=O)O

Precursor

UITKHKNFVCYWNG-UHFFFAOYSA-N

Benzophenonetetracarboxylic acid

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

Environmental

Downstream Successor

GMFRFZZDPCJNLU-UHFFFAOYSA-N

C(=O)(c1c(cc(cc1)C(=O)c2ccc(c(c2O)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

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

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