Search More · GCI-TPs

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

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

12 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

8 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

11 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

17 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

17 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

17 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.

Upstream Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

OAHLLHJOPUWLKW-UHFFFAOYSA-N

5,8-Dihydro-1-naphthol

C1C=CCC2=C1C=CC=C2O

Environmental

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

MMODIROKOSLUHP-UHFFFAOYSA-N

1-((5,8-Dihydro-1-naphthyl)oxy)-3-(isopropylamino)propan-2-ol

CC(C)NCC(COC1=CC=CC2=C1CC=CC2)O

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

MMODIROKOSLUHP-UHFFFAOYSA-N

1-((5,8-Dihydro-1-naphthyl)oxy)-3-(isopropylamino)propan-2-ol

CC(C)NCC(COC1=CC=CC2=C1CC=CC2)O

Environmental

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

YCETZYXKHCVZDL-UHFFFAOYSA-N

4-(Methyloctadecylamino)-3-((5,6,7,8-tetrahydro-1-hydroxy-2-naphthyl)carbamoyl)benzenesulphonic acid

CCCCCCCCCCCCCCCCCCN(C)C1=C(C=CC(=C1)S(=O)(=O)O)NC(=O)C2=C(C3=…

Environmental

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

YCETZYXKHCVZDL-UHFFFAOYSA-N

4-(Methyloctadecylamino)-3-((5,6,7,8-tetrahydro-1-hydroxy-2-naphthyl)carbamoyl)benzenesulphonic acid

CCCCCCCCCCCCCCCCCCN(C)C1=C(C=CC(=C1)S(=O)(=O)O)NC(=O)C2=C(C3=…

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

SODWJACROGQSMM-UHFFFAOYSA-N

5-Tetralinylamine

C1CCC2=C(C1)C=CC=C2N

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

VXZHOWCMXKLZNY-UHFFFAOYSA-N

1,2,3,4-Tetrahydro-5-nitronaphthalene

C1CCC2=C(C1)C=CC=C2[N+](=O)[O-]

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

VXZHOWCMXKLZNY-UHFFFAOYSA-N

1,2,3,4-Tetrahydro-5-nitronaphthalene

C1CCC2=C(C1)C=CC=C2[N+](=O)[O-]

Environmental

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Upstream Precursor

VXZHOWCMXKLZNY-UHFFFAOYSA-N

1,2,3,4-Tetrahydro-5-nitronaphthalene

C1CCC2=C(C1)C=CC=C2[N+](=O)[O-]

Abiotic

Product

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

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

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

CNOYQLOSBYLHEK-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,2-diol

C1CCc2c(C1)ccc(c2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

CNOYQLOSBYLHEK-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,2-diol

C1CCc2c(C1)ccc(c2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Environmental

Downstream Successor

CNOYQLOSBYLHEK-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,2-diol

C1CCc2c(C1)ccc(c2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Environmental

Downstream Successor

DFENWDLABYQUIC-UHFFFAOYSA-N

C1CC2=C(C(=CC=C2CC1O)O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

DFENWDLABYQUIC-UHFFFAOYSA-N

C1CC2=C(C(=CC=C2CC1O)O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

LVBXYWRVNMXVMT-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,3-diol

C1CCc2c(C1)cc(cc2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

GVTDRUXHMYZTFF-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1,4-naphthalenediol

C1CCC2=C(C1)C(O)=CC=C2O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Environmental

Downstream Successor

RLPCSMSHLXZWNJ-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,6-diol

C1(CCc2c(C1)cccc2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Environmental

Downstream Successor

LNLGJFLOBBEUPK-UHFFFAOYSA-N

5,6,7,8-Tetrahydronaphthalene-1,7-diol

C1C(Cc2c(C1)cccc2O)O

Precursor

SCWNNOCLLOHZIG-UHFFFAOYSA-N

5,6,7,8-Tetrahydro-1-naphthol

Oc1cccc2c1CCCC2

Abiotic

Downstream Successor

DUQUFSQRQYYYBG-UHFFFAOYSA-N

4-Chloro-5,6,7,8-tetrahydronaphthalen-1-ol

C1CCC2=C(C1)C(=CC=C2O)Cl

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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