Search More · GCI-TPs

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

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

16 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

16 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

3 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

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

Upstream Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

ZTQJSJLZARPEBW-UHFFFAOYSA-N

Ethyl 2-(m-nitrophenylmethylene)-4-chloro-3-oxobutanoate

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

Environmental

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

ZTQJSJLZARPEBW-UHFFFAOYSA-N

Ethyl 2-(m-nitrophenylmethylene)-4-chloro-3-oxobutanoate

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

Abiotic

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

ZTQJSJLZARPEBW-UHFFFAOYSA-N

Ethyl 2-(m-nitrophenylmethylene)-4-chloro-3-oxobutanoate

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

Abiotic

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

ZTQJSJLZARPEBW-UHFFFAOYSA-N

Ethyl 2-(m-nitrophenylmethylene)-4-chloro-3-oxobutanoate

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

Environmental

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

SKSVQBBQJHUOSX-UHFFFAOYSA-N

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

Abiotic

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Upstream Precursor

SKSVQBBQJHUOSX-UHFFFAOYSA-N

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

Environmental

Product

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

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

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Environmental

Downstream Successor

KICCIGJFMGOSKO-UHFFFAOYSA-N

Butanoic acid, 2-[(2,3-dihydroxyphenyl)methylene]-3-oxo-

OC(=O)C(=CC1=C(C(=CC=C1)O)O)C(=O)C

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Downstream Successor

KICCIGJFMGOSKO-UHFFFAOYSA-N

Butanoic acid, 2-[(2,3-dihydroxyphenyl)methylene]-3-oxo-

OC(=O)C(=CC1=C(C(=CC=C1)O)O)C(=O)C

Precursor

YOPMSDPIOQUWFE-UHFFFAOYSA-N

Ethyl 2-(3-nitrobenzylidene)-3-oxobutanoate

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

Abiotic

Downstream Successor

QXLGUWJCTSGSDB-UHFFFAOYSA-N

Nimodipine Impurity N15

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

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

No Original Precursors

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