Search More · GCI-TPs

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

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

6 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

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

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

C(=O)(C1=C(C=C2C=CC=CC2=C1)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Environmental

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

C(=O)(C1=C(C=C2C=CC=CC2=C1)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Environmental

Downstream Successor

PRRZDZJYSJLDBS-UHFFFAOYSA-N

Bromopyruvic Acid

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

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Abiotic

Downstream Successor

YLDFTMJPQJXGSS-UHFFFAOYSA-N

6-Bromo-2-naphthalenol

C1=C(C=C2C=CC(=CC2=C1)Br)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Environmental

Downstream Successor

YLDFTMJPQJXGSS-UHFFFAOYSA-N

6-Bromo-2-naphthalenol

C1=C(C=C2C=CC(=CC2=C1)Br)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Abiotic

Downstream Successor

XZWXQSGFZHRDNB-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy-

C(=O)(C1=C(C=C2C=CC(=CC2=C1)Br)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Environmental

Downstream Successor

XZWXQSGFZHRDNB-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 7-bromo-3-hydroxy-

C(=O)(C1=C(C=C2C=CC(=CC2=C1)Br)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Environmental

Downstream Successor

BAZKPXAACOAELY-UHFFFAOYSA-N

6-Bromonaphthalene-2,3-diol

c1(c(cc2ccc(cc2c1)Br)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Abiotic

Downstream Successor

BAZKPXAACOAELY-UHFFFAOYSA-N

6-Bromonaphthalene-2,3-diol

c1(c(cc2ccc(cc2c1)Br)O)O

Precursor

WNMKUIQCIRAXBN-UHFFFAOYSA-N

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

C1=CC2=C(C(=C(C=C2C=C1Br)C(=O)O)O)Br

Abiotic

Downstream Successor

XMLACAICHWPIJR-UHFFFAOYSA-N

4-Bromo-2-(2-carboxyethenyl)benzoic acid

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

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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