Search More · GCI-TPs

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

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

9 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

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

Upstream Precursor

JBAUEKOSVODIKJ-UHFFFAOYSA-N

CCOC(=O)CC(NNC1=C(C=C(C=C1Cl)Cl)Cl)=O

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

JBAUEKOSVODIKJ-UHFFFAOYSA-N

CCOC(=O)CC(NNC1=C(C=C(C=C1Cl)Cl)Cl)=O

Abiotic

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

JBAUEKOSVODIKJ-UHFFFAOYSA-N

CCOC(=O)CC(NNC1=C(C=C(C=C1Cl)Cl)Cl)=O

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

ZIUSEGSNTOUIPT-UHFFFAOYSA-N

Ethyl cyanoacetate

CCOC(CC#N)=O

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

ZIUSEGSNTOUIPT-UHFFFAOYSA-N

Ethyl cyanoacetate

CCOC(CC#N)=O

Abiotic

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

HNTAACUZDYAMHO-UHFFFAOYSA-N

Ethyl 3-(5-amino-2-chloroanilino)-3-[2-(2,4,6-trichlorophenyl)hydrazinylidene]propanoate

CCOC(=O)CC(=NC1=C(C=CC(=C1)N)Cl)NNC2=C(C=C(C=C2Cl)Cl)Cl

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

BZJRKACJPRTFNO-UHFFFAOYSA-N

CCOC(=O)C(C(C#N)(C(=O)O)O)C#N

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

IMFDUANUXOSYEE-UHFFFAOYSA-N

Ethyl 3-[(2-chloro-5-nitrophenyl)imino]-3-[2-(2,4,6-trichlorophenyl)hydrazino]propanoate

CCOC(=O)CC(=NC1=C(C=CC(=C1)[N+](=O)[O-])Cl)NNC2=C(C=C(C=C2Cl)Cl)Cl

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

IQWJYGDCWITXMW-UHFFFAOYSA-N

CCOC(=O)CC(NNC1=C(C=C(C=C1O)Cl)Cl)=O

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Upstream Precursor

IZUYLTCDLDDGQD-UHFFFAOYSA-N

Propanoic acid, 3-((4-nitrophenyl)amino)-3-(2-(2,4,6-trichlorophenyl)hydrazinylidene)-, ethyl ester

CCOC(=O)CC(=NC1=CC=C(C=C1)[N+](=O)[O-])NNC2=C(C=C(C=C2Cl)Cl)Cl

Environmental

Product

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

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

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Abiotic

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Environmental

Downstream Successor

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Acetamide

NC(=O)C

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Abiotic

Downstream Successor

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Acetamide

NC(=O)C

Precursor

UVSPVEYCSVXYBB-UHFFFAOYSA-N

Ethyl 2-carbamoylacetate

CCOC(=O)CC(N)=O

Abiotic

Downstream Successor

CGJMROBVSBIBKP-UHFFFAOYSA-N

3-Amino-3-Oxopropanoic Acid

NC(=O)CC(=O)O

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

No Original Precursors

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