Search More · GCI-TPs

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

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

17 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.

Upstream Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Product

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Upstream Precursor

PJIJWAPIIFKMCY-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)Cl)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Product

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Upstream Precursor

PJIJWAPIIFKMCY-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)Cl)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Product

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Upstream Precursor

PJIJWAPIIFKMCY-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)Cl)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Product

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Upstream Precursor

PJIJWAPIIFKMCY-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)Cl)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Product

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Previewing top 5 entries. If you want the full results, please use the download button above.

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Downstream Successor

MHERFNGTCNVCDD-UHFFFAOYSA-N

C(C(=NO)C1=CC=CC=C1Cl)(O)=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

MHERFNGTCNVCDD-UHFFFAOYSA-N

C(C(=NO)C1=CC=CC=C1Cl)(O)=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

OSNLFPWOJQJHEP-UHFFFAOYSA-N

CC(C)CCCCCCC(C=C(C(O)=O)C(=NO)C1=CC=CC=C1Cl)=CC(O)=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Downstream Successor

OSNLFPWOJQJHEP-UHFFFAOYSA-N

CC(C)CCCCCCC(C=C(C(O)=O)C(=NO)C1=CC=CC=C1Cl)=CC(O)=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

OSNLFPWOJQJHEP-UHFFFAOYSA-N

CC(C)CCCCCCC(C=C(C(O)=O)C(=NO)C1=CC=CC=C1Cl)=CC(O)=O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

UVSSQXLTISBLOC-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=C(C=C2Cl)O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Abiotic

Downstream Successor

KOJOXCJMBZEIGZ-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)O)O)C(=NO)C2=CC=CC=C2Cl

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Downstream Successor

GJFKFZUAZQPFLI-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2O

Precursor

BGNZDRWQKYSHJP-UHFFFAOYSA-N

2-[C-(2-chlorophenyl)-N-hydroxycarbonimidoyl]-4-(7-methyloctyl)phenol

CC(C)CCCCCCC1=CC(=C(C=C1)O)C(=NO)C2=CC=CC=C2Cl

Environmental

Downstream Successor

KOJOXCJMBZEIGZ-UHFFFAOYSA-N

CC(C)CCCCCCC1=CC(=C(C(=C1)O)O)C(=NO)C2=CC=CC=C2Cl

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

No Original Precursors

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