Search More · GCI-TPs

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

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.

Upstream Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

QUNVBZBEOIMRIE-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 6-amino-5-[2-[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-4-hydroxy-

C1=CC(=C(C2=C(C=C(C=C21)S(=O)(=O)O)O)N=NC3=C(C=C(C=C3)Cl)C(F)(F)F)N

Abiotic

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

QUNVBZBEOIMRIE-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 6-amino-5-[2-[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-4-hydroxy-

C1=CC(=C(C2=C(C=C(C=C21)S(=O)(=O)O)O)N=NC3=C(C=C(C=C3)Cl)C(F)(F)F)N

Environmental

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

QUNVBZBEOIMRIE-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 6-amino-5-[2-[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-4-hydroxy-

C1=CC(=C(C2=C(C=C(C=C21)S(=O)(=O)O)O)N=NC3=C(C=C(C=C3)Cl)C(F)(F)F)N

Abiotic

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

QUNVBZBEOIMRIE-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 6-amino-5-[2-[4-chloro-2-(trifluoromethyl)phenyl]diazenyl]-4-hydroxy-

C1=CC(=C(C2=C(C=C(C=C21)S(=O)(=O)O)O)N=NC3=C(C=C(C=C3)Cl)C(F)(F)F)N

Environmental

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

MAQUEEQQMCTREP-UHFFFAOYSA-N

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

Abiotic

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

MAQUEEQQMCTREP-UHFFFAOYSA-N

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

Environmental

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

MAQUEEQQMCTREP-UHFFFAOYSA-N

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

Abiotic

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

MAQUEEQQMCTREP-UHFFFAOYSA-N

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

Environmental

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Upstream Precursor

WEFICEHFAFVHKA-UHFFFAOYSA-N

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

Environmental

Product

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

XPDWGBQVDMORPB-UHFFFAOYSA-N

Trifluoromethane

C(F)(F)F

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

AWZDHMJWNNLOIV-UHFFFAOYSA-N

5,6-Diamino-4-hydroxynaphthalene-2-sulfonic acid

S(=O)(=O)(C1=CC(=C2C(=C1)C=CC(=C2N)N)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Environmental

Downstream Successor

AWZDHMJWNNLOIV-UHFFFAOYSA-N

5,6-Diamino-4-hydroxynaphthalene-2-sulfonic acid

S(=O)(=O)(C1=CC(=C2C(=C1)C=CC(=C2N)N)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

AWZDHMJWNNLOIV-UHFFFAOYSA-N

5,6-Diamino-4-hydroxynaphthalene-2-sulfonic acid

S(=O)(=O)(C1=CC(=C2C(=C1)C=CC(=C2N)N)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

BUTHMSUEBYPMKJ-UHFFFAOYSA-N

3-Sulfopyruvic acid

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

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

CZWSAXNDCOPCAP-UHFFFAOYSA-N

5-Amino-4,6-dihydroxynaphthalene-2-sulfonic acid

NC1=C(C=CC2=CC(=CC(=C21)O)S(=O)(=O)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Environmental

Downstream Successor

CZWSAXNDCOPCAP-UHFFFAOYSA-N

5-Amino-4,6-dihydroxynaphthalene-2-sulfonic acid

NC1=C(C=CC2=CC(=CC(=C21)O)S(=O)(=O)O)O

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

VBLXCTYLWZJBKA-UHFFFAOYSA-N

2-(Trifluoromethyl)aniline

Nc1c(cccc1)C(F)(F)F

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Environmental

Downstream Successor

VBLXCTYLWZJBKA-UHFFFAOYSA-N

2-(Trifluoromethyl)aniline

Nc1c(cccc1)C(F)(F)F

Precursor

DIAXRUOBYBLEJE-UHFFFAOYSA-N

Acid Red 337 free acid

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

Abiotic

Downstream Successor

AQNYJBKPOPUIHV-UHFFFAOYSA-N

2-Naphthalenesulfonic acid, 6-amino-4-hydroxy-5-(phenylazo)-

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

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

No Original Precursors

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