Search More · GCI-TPs

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

8 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)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.

Upstream Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Product

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Upstream Precursor

BVFDBEYZBUIFNR-UHFFFAOYSA-N

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C(=C3)Cl)C(=CC=C4)S(=O)(=O)O)O

Environmental

Product

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Upstream Precursor

BVFDBEYZBUIFNR-UHFFFAOYSA-N

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C(=C3)Cl)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Product

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Upstream Precursor

BVFDBEYZBUIFNR-UHFFFAOYSA-N

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C(=C3)Cl)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Product

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Upstream Precursor

BVFDBEYZBUIFNR-UHFFFAOYSA-N

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C(=C3)Cl)C(=CC=C4)S(=O)(=O)O)O

Environmental

Product

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

C1(=C(N)C2=CC=CC=C2C=C1)O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Environmental

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

C1(=C(N)C2=CC=CC=C2C=C1)O

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

RUFPHBVGCFYCNW-UHFFFAOYSA-N

1-Naphthylamine

c1cc2ccccc2c(c1)N

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Environmental

Downstream Successor

RUFPHBVGCFYCNW-UHFFFAOYSA-N

1-Naphthylamine

c1cc2ccccc2c(c1)N

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

RUFPHBVGCFYCNW-UHFFFAOYSA-N

1-Naphthylamine

c1cc2ccccc2c(c1)N

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Environmental

Downstream Successor

VRRRFZAFEQBWAS-UHFFFAOYSA-N

2,3-Dihydroxy-1-naphthylamine

OC1=C(C2=CC=CC=C2C=C1O)N

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

VRRRFZAFEQBWAS-UHFFFAOYSA-N

2,3-Dihydroxy-1-naphthylamine

OC1=C(C2=CC=CC=C2C=C1O)N

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

ABJQKDJOYSQVFX-UHFFFAOYSA-N

1-Amino-4-naphthol

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Environmental

Downstream Successor

ABJQKDJOYSQVFX-UHFFFAOYSA-N

1-Amino-4-naphthol

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

Precursor

AMEWLVLJCCOGDI-UHFFFAOYSA-N

5-Hydroxy-6-[2-(1-naphthalenyl)diazenyl]-1-naphthalenesulfonic acid

C1=CC=C2C(=C1)C=CC=C2N=NC3=C(C4=C(C=C3)C(=CC=C4)S(=O)(=O)O)O

Abiotic

Downstream Successor

ABJQKDJOYSQVFX-UHFFFAOYSA-N

1-Amino-4-naphthol

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

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

No Original Precursors

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