Search More · GCI-TPs

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

6 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

11 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

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Product

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Upstream Precursor

JXRDPKSVJFQNGK-UHFFFAOYSA-N

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C(=CC3=CC=CC=C32)Cl)O

Abiotic

Product

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Upstream Precursor

JXRDPKSVJFQNGK-UHFFFAOYSA-N

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C(=CC3=CC=CC=C32)Cl)O

Environmental

Product

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Upstream Precursor

JXRDPKSVJFQNGK-UHFFFAOYSA-N

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C(=CC3=CC=CC=C32)Cl)O

Environmental

Product

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Upstream Precursor

JXRDPKSVJFQNGK-UHFFFAOYSA-N

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C(=CC3=CC=CC=C32)Cl)O

Abiotic

Product

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Environmental

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Environmental

Downstream Successor

FHMMQQXRSYSWCM-UHFFFAOYSA-N

1-Amino-2-naphthol

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Environmental

Downstream Successor

VRRRFZAFEQBWAS-UHFFFAOYSA-N

2,3-Dihydroxy-1-naphthylamine

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Downstream Successor

VRRRFZAFEQBWAS-UHFFFAOYSA-N

2,3-Dihydroxy-1-naphthylamine

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

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Downstream Successor

NXPPAOGUKPJVDI-UHFFFAOYSA-N

1,2-Dihydroxynaphthalene

c1cc2ccccc2c(c1O)O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Environmental

Downstream Successor

NXPPAOGUKPJVDI-UHFFFAOYSA-N

1,2-Dihydroxynaphthalene

c1cc2ccccc2c(c1O)O

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Abiotic

Downstream Successor

CBIATSACMOQCIA-UHFFFAOYSA-N

1-Amino-3-chloronaphthalen-2-ol

OC1=C(C2=CC=CC=C2C=C1Cl)N

Precursor

ZNRKXQFZAHYEIW-UHFFFAOYSA-N

5-Chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-propan-2-ylbenzenesulfonic acid

CC(C)C1=CC(=C(C=C1Cl)S(=O)(=O)O)N=NC2=C(C=CC3=CC=CC=C32)O

Environmental

Downstream Successor

CBIATSACMOQCIA-UHFFFAOYSA-N

1-Amino-3-chloronaphthalen-2-ol

OC1=C(C2=CC=CC=C2C=C1Cl)N

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.