Search More · GCI-TPs

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

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

12 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

12 steps

Dead-End Product

CPRDLBPDNZTCSM-UHFFFAOYSA-N

But-1-ene-1,1-diol

CCC=C(O)O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

9 steps

Dead-End Product

CJXCLBPFKGZXJP-UHFFFAOYSA-N

4,5-Dideoxypentonic acid

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

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

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Environmental

Downstream Successor

JKCJGCLCFORONP-UHFFFAOYSA-N

CC(=C(O)C(=O)O)C(=CC(O)=O)NN=C1C=CC(=O)C(=NNC2=CC=CC=C2C)C1=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

HFMKDGHUNOPVAA-UHFFFAOYSA-N

2,5-Dimethylphenylhydroxylamine

CC1=CC(=C(C=C1)C)NO

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

BSFHJMGROOFSRA-UHFFFAOYSA-N

Nitro-p-xylene

CC1=C(C=C(C=C1)C)[N+](=O)[O-]

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

KXANPQAYQCSNFR-UHFFFAOYSA-N

1,4-Dimethyl-2-nitrosobenzene

Cc1cc(c(cc1)C)N=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Environmental

Downstream Successor

JWPFJENSNJLHEI-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC(=C(C=C3C)O)O)C2=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

JWPFJENSNJLHEI-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC(=C(C=C3C)O)O)C2=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

JWPFJENSNJLHEI-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC(=C(C=C3C)O)O)C2=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Abiotic

Downstream Successor

MOBNMJSVQHYINQ-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=C(C(=CC=C3C)O)O)C2=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Environmental

Downstream Successor

JWPFJENSNJLHEI-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC(=C(C=C3C)O)O)C2=O

Precursor

AZTRKCIWOMTGDN-UHFFFAOYSA-N

6-[(2,5-Dimethylphenyl)hydrazinylidene]-2-[(2-methylphenyl)hydrazinylidene]cyclohex-4-ene-1,3-dione

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=CC=CC=C3C)C2=O

Environmental

Downstream Successor

MOBNMJSVQHYINQ-UHFFFAOYSA-N

CC1=CC(=C(C=C1)C)NN=C2C=CC(=O)C(=NNC3=C(C(=CC=C3C)O)O)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.

No All Precursors

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

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