Search More · GCI-TPs

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

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

9 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

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

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Abiotic

Downstream Successor

FUXMTEKFGUWSNC-UHFFFAOYSA-N

2,3,4,5-Tetrachlorobenzoic Acid

C(C1=CC(=C(C(=C1Cl)Cl)Cl)Cl)(O)=O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Environmental

Downstream Successor

FUXMTEKFGUWSNC-UHFFFAOYSA-N

2,3,4,5-Tetrachlorobenzoic Acid

C(C1=CC(=C(C(=C1Cl)Cl)Cl)Cl)(O)=O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Abiotic

Downstream Successor

WZHHYIOUKQNLQM-UHFFFAOYSA-N

Tetrachlorophthalic acid

C1(=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)O)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Environmental

Downstream Successor

TXKNLOLDXXHOAP-UHFFFAOYSA-N

3,4,6-Trichloro-5-hydroxyphthalic acid

OC(=O)c1c(c(c(c(c1Cl)O)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Abiotic

Downstream Successor

TXKNLOLDXXHOAP-UHFFFAOYSA-N

3,4,6-Trichloro-5-hydroxyphthalic acid

OC(=O)c1c(c(c(c(c1Cl)O)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Abiotic

Downstream Successor

DCACTBQREATMLX-UHFFFAOYSA-N

3,4,6-trichlorophthalic Acid

OC(=O)C1=C(C(=C(C=C1Cl)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Environmental

Downstream Successor

DCACTBQREATMLX-UHFFFAOYSA-N

3,4,6-trichlorophthalic Acid

OC(=O)C1=C(C(=C(C=C1Cl)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Abiotic

Downstream Successor

QGXQXRTVKOXDDC-UHFFFAOYSA-N

Benzenedicarboxylic acid, trichloro-

OC(=O)C1=C(C(=C(C(=C1)Cl)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Environmental

Downstream Successor

QGXQXRTVKOXDDC-UHFFFAOYSA-N

Benzenedicarboxylic acid, trichloro-

OC(=O)C1=C(C(=C(C(=C1)Cl)Cl)Cl)C(=O)O

Precursor

LSXSFYOXBYEKGC-UHFFFAOYSA-N

Benzoic acid, 2-(1H-benzimidazol-1-ylcarbonyl)-3,4,5,6-tetrachloro-

C1=CC=C2C(=C1)N=CN2C(=O)C3=C(C(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)O

Environmental

Downstream Successor

UQACMDQCBRCZSU-UHFFFAOYSA-N

OC(=O)C1=C(C(=C(C(=C1O)Cl)Cl)Cl)C(=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.

No All Precursors

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

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