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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

4 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

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

AUWXOLNGLLHZEO-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)…

Environmental

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

AUWXOLNGLLHZEO-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)…

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

FIOROMAJRWPHLV-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC(=C(C=C3)O)Cl)[N+]…

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

FIOROMAJRWPHLV-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC(=C(C=C3)O)Cl)[N+]…

Environmental

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

AUWXOLNGLLHZEO-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)…

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

AUWXOLNGLLHZEO-UHFFFAOYSA-N

C1=C(C(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)…

Environmental

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

KOTPXGVWNCPULC-UHFFFAOYSA-N

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC(=C(C=C3)O)Cl)[N+](…

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

KOTPXGVWNCPULC-UHFFFAOYSA-N

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC(=C(C=C3)O)Cl)[N+](…

Environmental

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Upstream Precursor

KOTPXGVWNCPULC-UHFFFAOYSA-N

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC(=C(C=C3)O)Cl)[N+](…

Abiotic

Product

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Environmental

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

KDHUXRBROABJBC-UHFFFAOYSA-N

4-Aminocatechol

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Environmental

Downstream Successor

KDHUXRBROABJBC-UHFFFAOYSA-N

4-Aminocatechol

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

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

JSTCPNFNKICNNO-UHFFFAOYSA-N

4-Nitrosophenol

C1=CC(=CC=C1O)N=O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

DMEOYBXJWVYCNP-UHFFFAOYSA-N

(4-Hydroxyphenyl)sulfamic acid

Oc1ccc(cc1)NS(=O)(=O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Environmental

Downstream Successor

DMEOYBXJWVYCNP-UHFFFAOYSA-N

(4-Hydroxyphenyl)sulfamic acid

Oc1ccc(cc1)NS(=O)(=O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

DMEOYBXJWVYCNP-UHFFFAOYSA-N

(4-Hydroxyphenyl)sulfamic acid

Oc1ccc(cc1)NS(=O)(=O)O

Precursor

BZMNJADAIGWBPM-UHFFFAOYSA-N

N-(4-Hydroxyphenyl)-4-((4-hydroxyphenyl)amino)-3-nitrobenzenesulphonamide

C1=CC(=CC=C1NC2=C(C=C(C=C2)S(=O)(=O)NC3=CC=C(C=C3)O)[N+](=O)[O-])O

Abiotic

Downstream Successor

HLYUNLCPAMQQGC-UHFFFAOYSA-N

OC1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)O)[N+](=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.

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