Search More · GCI-TPs

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

Upstream Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

FQZICXNEDHUJQD-UHFFFAOYSA-O

C1CSC(=N)[NH+]1CC(=O)C2=CC(=CC=C2)[N+](=O)[O-]

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

FQZICXNEDHUJQD-UHFFFAOYSA-O

C1CSC(=N)[NH+]1CC(=O)C2=CC(=CC=C2)[N+](=O)[O-]

Environmental

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

FQZICXNEDHUJQD-UHFFFAOYSA-O

C1CSC(=N)[NH+]1CC(=O)C2=CC(=CC=C2)[N+](=O)[O-]

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

FQZICXNEDHUJQD-UHFFFAOYSA-O

C1CSC(=N)[NH+]1CC(=O)C2=CC(=CC=C2)[N+](=O)[O-]

Environmental

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

MGGSVGVOLYKRAF-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C2=CC(=CC=C2)O

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

MGGSVGVOLYKRAF-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C2=CC(=CC=C2)O

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

MGGSVGVOLYKRAF-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C2=CC(=CC=C2)O

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Upstream Precursor

BWBNCWBMASOYQZ-UHFFFAOYSA-O

2-(2-Amino-4,5-dihydro-1,3-thiazol-3-ium-3-yl)-1-phenylethanone

C1CSC(=N)[NH+]1CC(=O)C2=CC=CC=C2

Abiotic

Product

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

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

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

REGFWZVTTFGQOJ-UHFFFAOYSA-N

4,5-Dihydro-2-thiazolamine

C1CSC(=N)N1

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Environmental

Downstream Successor

REGFWZVTTFGQOJ-UHFFFAOYSA-N

4,5-Dihydro-2-thiazolamine

C1CSC(=N)N1

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

REGFWZVTTFGQOJ-UHFFFAOYSA-N

4,5-Dihydro-2-thiazolamine

C1CSC(=N)N1

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

KQAABIJAPSVCBR-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C(=CC(O)=O)C=CC(O)=O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Environmental

Downstream Successor

KQAABIJAPSVCBR-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C(=CC(O)=O)C=CC(O)=O

Precursor

CWFYNLZIQFUZPL-UHFFFAOYSA-N

1-(3,4-Dihydroxyphenyl)-2-(2-imino-1,3-thiazolan-3-YL)-1-ethanone

C1CSC(=N)N1CC(=O)C2=CC(=C(C=C2)O)O

Abiotic

Downstream Successor

DOESZVANVQGHLO-UHFFFAOYSA-N

C1CSC(=N)N1CC(=O)C2=C(C(=C(C=C2)O)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.

No Dead-Ends

No entries were found for this section with the current query and depth.

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