Search More · GCI-TPs

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Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

6 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

11 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

IZPUDUNKMAMNJZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-[2-(tetrabromochlorophenoxy)ethoxy]-

C(COC1=C(C(=C(C(=C1Br)Br)Br)Br)Br)OC2=C(C(=C(C(=C2Br)Br)Br)Br)Cl

Abiotic

Product

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Upstream Precursor

IZPUDUNKMAMNJZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-[2-(tetrabromochlorophenoxy)ethoxy]-

C(COC1=C(C(=C(C(=C1Br)Br)Br)Br)Br)OC2=C(C(=C(C(=C2Br)Br)Br)Br)Cl

Environmental

Product

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

SVHOVVJFOWGYJO-UHFFFAOYSA-N

Pentabromophenol

C1(=C(C(=C(C(=C1Br)Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Environmental

Downstream Successor

SVHOVVJFOWGYJO-UHFFFAOYSA-N

Pentabromophenol

C1(=C(C(=C(C(=C1Br)Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Environmental

Downstream Successor

KXZRECGEDVBJPM-UHFFFAOYSA-N

2,3,4,5-Tetrabromophenol

C1(=CC(=C(C(=C1Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

KXZRECGEDVBJPM-UHFFFAOYSA-N

2,3,4,5-Tetrabromophenol

C1(=CC(=C(C(=C1Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Environmental

Downstream Successor

CXPJZISGVIVNEL-UHFFFAOYSA-N

2,3,4,6-Tetrabromophenol

C1(=C(C(=C(C=C1Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

CXPJZISGVIVNEL-UHFFFAOYSA-N

2,3,4,6-Tetrabromophenol

C1(=C(C(=C(C=C1Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

ZANXWPPILUXIGV-UHFFFAOYSA-N

Ethanol, 2-(2,3,4,5,6-pentabromophenoxy)-

C(COC1=C(C(=C(C(=C1Br)Br)Br)Br)Br)O

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

RHFAFCQUXGORNZ-UHFFFAOYSA-N

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCO

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Abiotic

Downstream Successor

AQABUAVVCBXKEB-UHFFFAOYSA-N

C(COC1=C(C(=C(C=C1Br)Br)Br)Br)OC2=CC(=C(C(=C2Br)Br)Br)Br

Precursor

GFUDECFZQUUKCZ-UHFFFAOYSA-N

Benzene, 1,2,3,4,5-pentabromo-6-(2-(tetrabromophenoxy)ethoxy)-

C1=C(C(=C(C(=C1Br)Br)Br)Br)OCCOC2=C(C(=C(C(=C2Br)Br)Br)Br)Br

Environmental

Downstream Successor

AQABUAVVCBXKEB-UHFFFAOYSA-N

C(COC1=C(C(=C(C=C1Br)Br)Br)Br)OC2=CC(=C(C(=C2Br)Br)Br)Br

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No Original Precursors

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