Search More · GCI-TPs

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Upstream Precursor

QMEYRRLFSLHNJG-UHFFFAOYSA-N

3H-Naphtho(1,2,3-de)quinoline-1-carboxylic acid, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-, ethyl ester

CCOC(=O)C1=C2C3=CC=CC=C3C(=O)C4=C(C=CC(=C42)N(C1=O)C)Br

Abiotic

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

QMEYRRLFSLHNJG-UHFFFAOYSA-N

3H-Naphtho(1,2,3-de)quinoline-1-carboxylic acid, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-, ethyl ester

CCOC(=O)C1=C2C3=CC=CC=C3C(=O)C4=C(C=CC(=C42)N(C1=O)C)Br

Environmental

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

HCSVFPRILZPUFL-UHFFFAOYSA-N

3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C#N

Abiotic

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

HCSVFPRILZPUFL-UHFFFAOYSA-N

3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C#N

Environmental

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

HCSVFPRILZPUFL-UHFFFAOYSA-N

3H-Naphtho[1,2,3-de]quinoline-1-carbonitrile, 6-bromo-2,7-dihydro-3-methyl-2,7-dioxo-

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C#N

Environmental

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

KMQYDMHOXIQSCL-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(N)=O

Abiotic

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Upstream Precursor

KMQYDMHOXIQSCL-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(N)=O

Environmental

Product

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Previewing top 7 entries. If you want the full results, please use the download button above.

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

NMPOQSRAGJIJBD-UHFFFAOYSA-N

C(=O)(C1=C2C3=CC=C(C=C3C(=O)C4=C(C=CC(=C42)N(C1=O)C)Br)O)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

PTYOAWBVOGTSGM-UHFFFAOYSA-N

C(=O)(C1=C2C3=CC(=CC=C3C(=O)C4=C(C=CC(=C42)N(C1=O)C)Br)O)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Environmental

Downstream Successor

OSXVSLMSGDEOBG-UHFFFAOYSA-N

C(=O)(C1=C2C3=CC=CC=C3C(=O)C4=C(C=CC(=C42)NC1=O)Br)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

CWSVULBQYHACOI-UHFFFAOYSA-N

C(=O)(C(=C1C2=CC=CC=C2C(=O)C3=C(C=CC(=C31)NC)Br)C(=O)O)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

YOGWOOHUEKDKAF-UHFFFAOYSA-N

C(=O)(C1=C2C3=CC=CC=C3C(=O)C4=C(C=C(C(=C42)N(C1=O)C)O)Br)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Abiotic

Downstream Successor

OYLJTVQURWFJEG-UHFFFAOYSA-N

14-Methyl-8,15-dioxo-14-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9(17),10,12-heptaene-16-carboxylic acid

C(=O)(C1=C2C3=CC=CC=C3C(=O)C4=CC=CC(=C42)N(C1=O)C)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Environmental

Downstream Successor

OYLJTVQURWFJEG-UHFFFAOYSA-N

14-Methyl-8,15-dioxo-14-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9(17),10,12-heptaene-16-carboxylic acid

C(=O)(C1=C2C3=CC=CC=C3C(=O)C4=CC=CC(=C42)N(C1=O)C)O

Precursor

NIHAEMOZVFCJOG-UHFFFAOYSA-N

CN1C2=C3C(=C(C=C2)Br)C(=O)C4=CC=CC=C4C3=C(C1=O)C(=O)O

Environmental

Downstream Successor

QTNAUUGQZYCWGQ-UHFFFAOYSA-N

3H-Naphtho[1,2,3-de]quinoline-2,7-dione, 6-bromo-3-methyl-

CN1C2=C3C(=CC1=O)C4=CC=CC=C4C(=O)C3=C(C=C2)Br

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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