Search More · GCI-TPs

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

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

11 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

17 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

17 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

5 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

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

RRRGNIDYMUNGFN-UHFFFAOYSA-O

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)[NH+](C1=O)C

Abiotic

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

RRRGNIDYMUNGFN-UHFFFAOYSA-O

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)[NH+](C1=O)C

Environmental

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

RRRGNIDYMUNGFN-UHFFFAOYSA-O

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)[NH+](C1=O)C

Abiotic

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

RRRGNIDYMUNGFN-UHFFFAOYSA-O

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)[NH+](C1=O)C

Environmental

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

IHEGLXCZXKZXBC-UHFFFAOYSA-N

CN1C(=O)C(=CC2=CC=C(C=C2)[N+](C)(C)[O-])C(=O)NC1=O

Environmental

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

IHEGLXCZXKZXBC-UHFFFAOYSA-N

CN1C(=O)C(=CC2=CC=C(C=C2)[N+](C)(C)[O-])C(=O)NC1=O

Abiotic

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

SFQRFHQXUVCZMC-UHFFFAOYSA-N

C[N+]1(C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O)[O-]

Environmental

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

SFQRFHQXUVCZMC-UHFFFAOYSA-N

C[N+]1(C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O)[O-]

Abiotic

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Upstream Precursor

IHEGLXCZXKZXBC-UHFFFAOYSA-N

CN1C(=O)C(=CC2=CC=C(C=C2)[N+](C)(C)[O-])C(=O)NC1=O

Environmental

Product

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

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

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Environmental

Downstream Successor

NAPLVLRBYHFCJP-UHFFFAOYSA-N

2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-((4-(dimethylamino)phenyl)methylene)-

CN(C)C1=CC=C(C=C1)C=C2C(=O)NC(=O)NC2=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

NAPLVLRBYHFCJP-UHFFFAOYSA-N

2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-((4-(dimethylamino)phenyl)methylene)-

CN(C)C1=CC=C(C=C1)C=C2C(=O)NC(=O)NC2=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Environmental

Downstream Successor

ZYULCNMNFCMPJV-UHFFFAOYSA-N

CN(C(=O)C(=CC1=CC=C(C=C1)N(C)C)C(=O)O)C(N)=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

ZYULCNMNFCMPJV-UHFFFAOYSA-N

CN(C(=O)C(=CC1=CC=C(C=C1)N(C)C)C(=O)O)C(N)=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

WPWCHINPXUIACC-UHFFFAOYSA-N

CNC(NC(C(C(=O)O)=CC1=CC=C(C=C1)N(C)C)=O)=O

Precursor

GFUZHTMFTUBOPD-UHFFFAOYSA-N

5-[[4-(Dimethylamino)phenyl]methylene]-1-methylbarbituric acid

CN1C(=O)C(=CC2=CC=C(C=C2)N(C)C)C(=O)NC1=O

Abiotic

Downstream Successor

GNJYSVUZUBVGBO-UHFFFAOYSA-N

CN1C(=O)C(=CC2=CC=C(C=C2)NC)C(=O)NC1=O

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

No Original Precursors

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