Search More · GCI-TPs

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

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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Upstream Precursor

VRDSLANGUUXLBO-UHFFFAOYSA-N

OC1=CC=C(C=C1)CN(C(C2=CC=C(C=C2)OC)=O)C3=NC4=C(C(=N3)OCC5=CC=…

Environmental

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

VRDSLANGUUXLBO-UHFFFAOYSA-N

OC1=CC=C(C=C1)CN(C(C2=CC=C(C=C2)OC)=O)C3=NC4=C(C(=N3)OCC5=CC=…

Abiotic

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

GWVKQRCWKCUQHR-UHFFFAOYSA-N

OC1=CC=C(C=C1)CNC2=NC3=C(C(=N2)OCC4=CC=CC=C4)N(C=C3Br)COCC5=C…

Abiotic

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

GWVKQRCWKCUQHR-UHFFFAOYSA-N

OC1=CC=C(C=C1)CNC2=NC3=C(C(=N2)OCC4=CC=CC=C4)N(C=C3Br)COCC5=C…

Environmental

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

HWUNWPQDMNOUEF-UHFFFAOYSA-O

COC1=CC=C(C=C1)C[NH+](CC2=CC=C(C=C2)OC)C3=NC4=C(C(=N3)OCC5=CC…

Abiotic

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

HWUNWPQDMNOUEF-UHFFFAOYSA-O

COC1=CC=C(C=C1)C[NH+](CC2=CC=C(C=C2)OC)C3=NC4=C(C(=N3)OCC5=CC…

Environmental

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

PDYDAOZSBSOAAM-UHFFFAOYSA-N

COc1ccc(cc1)CNc2nc3c(c(n2)OCc4ccccc4)n(cc3Br)COCc5ccccc5

Environmental

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

PDYDAOZSBSOAAM-UHFFFAOYSA-N

COc1ccc(cc1)CNc2nc3c(c(n2)OCc4ccccc4)n(cc3Br)COCc5ccccc5

Abiotic

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

PDYDAOZSBSOAAM-UHFFFAOYSA-N

COc1ccc(cc1)CNc2nc3c(c(n2)OCc4ccccc4)n(cc3Br)COCc5ccccc5

Environmental

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Upstream Precursor

PDYDAOZSBSOAAM-UHFFFAOYSA-N

COc1ccc(cc1)CNc2nc3c(c(n2)OCc4ccccc4)n(cc3Br)COCc5ccccc5

Abiotic

Product

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

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

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Abiotic

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Abiotic

Downstream Successor

BVJSUAQZOZWCKN-UHFFFAOYSA-N

4-Hydroxybenzyl Alcohol

OCC1=CC=C(C=C1)O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

BVJSUAQZOZWCKN-UHFFFAOYSA-N

4-Hydroxybenzyl Alcohol

OCC1=CC=C(C=C1)O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Environmental

Downstream Successor

CURLTUGMZLYLDI-UHFFFAOYSA-N

Carbon Dioxide

C(=O)=O

Precursor

TXHHAOVCCJMUNN-UHFFFAOYSA-N

5H-Pyrrolo3,2-dpyrimidin-2-amine, 7-bromo-4-(phenylmethoxy)-5-(phenylmethoxy)methyl-

C1=CC=C(C=C1)COCN2C=C(C3=C2C(=NC(=N3)N)OCC4=CC=CC=C4)Br

Abiotic

Downstream Successor

LFELPNODBDSREQ-UHFFFAOYSA-N

4-Oxocyclohexa-2,5-diene-1-carbaldehyde

C1(C=CC(C=O)C=C1)=O

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No Original Precursors

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

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