Search More · GCI-TPs

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Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

18 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

9 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

7 steps

Dead-End Product

HJEBWCDVXVPBRC-UHFFFAOYSA-N

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

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

Upstream Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

ZZTJMQPRKBNGNX-UHFFFAOYSA-N

Benzene, 1,1'-thiobis[4-nitro-

C1=CC(=CC=C1[N+](=O)[O-])SC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

ZZTJMQPRKBNGNX-UHFFFAOYSA-N

Benzene, 1,1'-thiobis[4-nitro-

C1=CC(=CC=C1[N+](=O)[O-])SC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

ZZTJMQPRKBNGNX-UHFFFAOYSA-N

Benzene, 1,1'-thiobis[4-nitro-

C1=CC(=CC=C1[N+](=O)[O-])SC2=CC=C(C=C2)[N+](=O)[O-]

Environmental

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

FOPAYJWJHKMOHS-UHFFFAOYSA-N

1,1'-Sulfinylbis(4-nitrobenzene)

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

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

FOPAYJWJHKMOHS-UHFFFAOYSA-N

1,1'-Sulfinylbis(4-nitrobenzene)

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

Environmental

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

FOPAYJWJHKMOHS-UHFFFAOYSA-N

1,1'-Sulfinylbis(4-nitrobenzene)

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

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

FOPAYJWJHKMOHS-UHFFFAOYSA-N

1,1'-Sulfinylbis(4-nitrobenzene)

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

Environmental

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

HHVCFCCCZYQKDD-UHFFFAOYSA-N

1-(4-Nitrophenyl)sulfanyl-4-nitrosobenzene

c1cc(ccc1N=O)Sc2ccc(cc2)[N+](=O)[O-]

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Upstream Precursor

DEAXTHCUWCJAEB-UHFFFAOYSA-N

C1=CC(=CC=C1[N+](=O)[O-])[S+](C2=CC=C(C=C2)[N+](=O)[O-])Cl

Abiotic

Product

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Environmental

Downstream Successor

NRPKPJKPJBPLIF-UHFFFAOYSA-N

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Downstream Successor

VPWNQTHUCYMVMZ-UHFFFAOYSA-N

Bisphenol S

C1(=CC=C(C=C1)S(=O)(=O)C2=CC=C(C=C2)O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Environmental

Downstream Successor

AAKBWTHKHIMSCL-UHFFFAOYSA-N

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

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Downstream Successor

OIAHFNSAOGZMIJ-UHFFFAOYSA-N

4-((4-Hydroxyphenyl)sulfonyl)benzene-1,2-diol

c1cc(ccc1S(=O)(=O)c2cc(c(cc2)O)O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Environmental

Downstream Successor

OIAHFNSAOGZMIJ-UHFFFAOYSA-N

4-((4-Hydroxyphenyl)sulfonyl)benzene-1,2-diol

c1cc(ccc1S(=O)(=O)c2cc(c(cc2)O)O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Environmental

Downstream Successor

BWYBLJSYDXDXCH-UHFFFAOYSA-N

NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(C(=C2)O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Downstream Successor

BWYBLJSYDXDXCH-UHFFFAOYSA-N

NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(C(=C2)O)O

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Environmental

Downstream Successor

MQJKPEGWNLWLTK-UHFFFAOYSA-N

Dapsone

C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Downstream Successor

MQJKPEGWNLWLTK-UHFFFAOYSA-N

Dapsone

C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N

Precursor

BVHNGWRPAFKGFP-UHFFFAOYSA-N

Bis(4-nitrophenyl) sulphone

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

Abiotic

Downstream Successor

PSHPCZGANRRQDN-UHFFFAOYSA-N

4-((4-Aminophenyl)sulfonyl)phenol

C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)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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