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Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

2 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

2 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

7 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

4 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

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

DOHZIJDJOSBJFP-UHFFFAOYSA-N

Methionine, N-(2,4-dinitrophenyl)-

CSCCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

DOHZIJDJOSBJFP-UHFFFAOYSA-N

Methionine, N-(2,4-dinitrophenyl)-

CSCCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

DOHZIJDJOSBJFP-UHFFFAOYSA-N

Methionine, N-(2,4-dinitrophenyl)-

CSCCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

DOHZIJDJOSBJFP-UHFFFAOYSA-N

Methionine, N-(2,4-dinitrophenyl)-

CSCCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

DOHZIJDJOSBJFP-UHFFFAOYSA-N

Methionine, N-(2,4-dinitrophenyl)-

CSCCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

KFPFJKADCNQPPQ-UHFFFAOYSA-N

DNP-DL-methionine sulfone

CS(=O)(CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-])=O

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Upstream Precursor

KFPFJKADCNQPPQ-UHFFFAOYSA-N

DNP-DL-methionine sulfone

CS(=O)(CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-])=O

Abiotic

Product

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

DOPJTDJKZNWLRB-UHFFFAOYSA-N

2-Amino-5-Nitrophenol

c1cc(cc(c1N)O)[N+](=O)[O-]

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

LXQOQPGNCGEELI-UHFFFAOYSA-N

2,4-Dinitroaniline

C1=C(C=C(C(=C1)N)[N+](=O)[O-])[N+](=O)[O-]

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

AHAXQHVMYJKNCT-UHFFFAOYSA-N

6-Nitrocatecholamine

OC1=C(C=CC(=C1O)[N+](=O)[O-])N

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

AEQYJPOZURHRIO-UHFFFAOYSA-N

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

VDCDWNDTNSWDFJ-UHFFFAOYSA-N

3,5-Dinitrocatechol

C1(=CC(=CC(=C1O)[N+](=O)[O-])[N+](=O)[O-])O

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

BPMUYBNBQXRDJP-UHFFFAOYSA-N

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

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

BQHNBLOQZVZJOM-UHFFFAOYSA-N

5-Amino-3-nitrobenzene-1,2-diol

OC1=C(C=C(C=C1O)N)[N+](=O)[O-]

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Abiotic

Downstream Successor

BQHNBLOQZVZJOM-UHFFFAOYSA-N

5-Amino-3-nitrobenzene-1,2-diol

OC1=C(C=C(C=C1O)N)[N+](=O)[O-]

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

QEFRNWWLZKMPFJ-UHFFFAOYSA-N

Methionine sulfoxide, DL-

C(=O)(C(CCS(C)=O)N)O

Precursor

FTOHDWRUZIRPDU-UHFFFAOYSA-N

DL-2-(2,4-Dinitroanilino)-4-(methylsulphinyl)butyric acid

CS(=O)CCC(C(=O)O)NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]

Environmental

Downstream Successor

BGTJNYIDTMUSKJ-UHFFFAOYSA-N

C1(=C(C(=C(C=C1[N+](=O)[O-])[N+](=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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