Search More · GCI-TPs

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

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

7 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

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Abiotic

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

TXXHDPDFNKHHGW-UHFFFAOYSA-N

2,4-Hexadienedioic acid, (2Z,4Z)-

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

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Abiotic

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

C1=CC(=C(C=C1)O)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

C1=CC(=C(C=C1)O)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

AKCRQHGQIJBRMN-UHFFFAOYSA-N

2-Chloroaniline

C1=CC=C(C(=C1)Cl)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Abiotic

Downstream Successor

AKCRQHGQIJBRMN-UHFFFAOYSA-N

2-Chloroaniline

C1=CC=C(C(=C1)Cl)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

AKCRQHGQIJBRMN-UHFFFAOYSA-N

2-Chloroaniline

C1=CC=C(C(=C1)Cl)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Abiotic

Downstream Successor

AKCRQHGQIJBRMN-UHFFFAOYSA-N

2-Chloroaniline

C1=CC=C(C(=C1)Cl)N

Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Environmental

Downstream Successor

VCJJAJXTFPNHON-UHFFFAOYSA-N

4-Amino-3-hydroxy-2-naphthoic acid

Nc1c(c(cc2ccccc21)C(=O)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.