Search More · GCI-TPs

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

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.

Upstream Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Product

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Upstream Precursor

BAVWZFCNQHFTKD-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C(=C3O)Cl

Abiotic

Product

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Environmental

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Environmental

Downstream Successor

ALKYHXVLJMQRLQ-UHFFFAOYSA-N

3-Hydroxy-2-naphthoic acid

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

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Environmental

Downstream Successor

JWAZRIHNYRIHIV-UHFFFAOYSA-N

2-Naphthol

C1=CC2=C(C=C1)C=C(C=C2)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Downstream Successor

JWAZRIHNYRIHIV-UHFFFAOYSA-N

2-Naphthol

C1=CC2=C(C=C1)C=C(C=C2)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Abiotic

Downstream Successor

BMHCSEJDJONPSF-UHFFFAOYSA-N

3,4-Dihydroxynaphthalene-2-carboxylic acid

C1(=C(C(=CC2=CC=CC=C21)C(=O)O)O)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Environmental

Downstream Successor

BMHCSEJDJONPSF-UHFFFAOYSA-N

3,4-Dihydroxynaphthalene-2-carboxylic acid

C1(=C(C(=CC2=CC=CC=C21)C(=O)O)O)O

Precursor

QVNLFTAJEJIVKH-UHFFFAOYSA-N

[2-[(3-Hydroxynaphthalene-2-carbonyl)amino]phenyl] 4-methylbenzenesulfonate

CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=CC=C2NC(=O)C3=CC4=CC=CC=C4C=C3O

Environmental

Downstream Successor

JRNGUTKWMSBIBF-UHFFFAOYSA-N

2,3-Dihydroxynaphthalene

C1(=CC2=CC=CC=C2C=C1O)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.