Search More · GCI-TPs

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Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

8 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

6 steps

Dead-End Product

ATRULDXOZAITDR-ARJAWSKDSA-N

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

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

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Environmental

Downstream Successor

CBCKQZAAMUWICA-UHFFFAOYSA-N

P-Phenylenediamine

Nc1ccc(cc1)N

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Abiotic

Downstream Successor

CBCKQZAAMUWICA-UHFFFAOYSA-N

P-Phenylenediamine

Nc1ccc(cc1)N

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Abiotic

Downstream Successor

KDHUXRBROABJBC-UHFFFAOYSA-N

4-Aminocatechol

OC1=C(C=CC(=C1)N)O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Environmental

Downstream Successor

KDHUXRBROABJBC-UHFFFAOYSA-N

4-Aminocatechol

OC1=C(C=CC(=C1)N)O

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Environmental

Downstream Successor

ZAJAQTYSTDTMCU-UHFFFAOYSA-M

3-Aminobenzenesulfonate

C1=CC=C(C=C1S(=O)(=O)[O-])N

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Abiotic

Downstream Successor

ZAJAQTYSTDTMCU-UHFFFAOYSA-M

3-Aminobenzenesulfonate

C1=CC=C(C=C1S(=O)(=O)[O-])N

Precursor

AWMKYVHXBRYAIP-UHFFFAOYSA-N

4-Chloro-3-[[4-(sulfomethylamino)phenyl]diazenyl]benzenesulfonic acid

C1=CC(=CC=C1NCS(=O)(=O)O)N=NC2=C(C=CC(=C2)S(=O)(=O)O)Cl

Abiotic

Downstream Successor

ULUIMLJNTCECJU-UHFFFAOYSA-M

3-Amino-4-hydroxybenzenesulfonate

C1=C(C(=CC(=C1)S(=O)(=O)[O-])N)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.

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