Search More · GCI-TPs

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

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

Upstream Precursor

SWVPEZYERZIFRI-UHFFFAOYSA-N

Benzene, (2,2-bis((1-ethenyl-1,5-dimethyl-4-hexen-1-yl)oxy)ethyl)-

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C=C)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

SWVPEZYERZIFRI-UHFFFAOYSA-N

Benzene, (2,2-bis((1-ethenyl-1,5-dimethyl-4-hexen-1-yl)oxy)ethyl)-

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C=C)C

Abiotic

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

SWVPEZYERZIFRI-UHFFFAOYSA-N

Benzene, (2,2-bis((1-ethenyl-1,5-dimethyl-4-hexen-1-yl)oxy)ethyl)-

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C=C)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

SWVPEZYERZIFRI-UHFFFAOYSA-N

Benzene, (2,2-bis((1-ethenyl-1,5-dimethyl-4-hexen-1-yl)oxy)ethyl)-

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C=C)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

RNMZAIOMSLDBJK-UHFFFAOYSA-N

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

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

NKOOHKQALQUESS-UHFFFAOYSA-N

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCCC(C)C)C2CO2)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

RNMZAIOMSLDBJK-UHFFFAOYSA-N

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

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

CCIGHTSEKACPKY-UHFFFAOYSA-N

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C2CO2)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

SUYDTPYZPUQXPZ-UHFFFAOYSA-N

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C(CO)Cl)C

Abiotic

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Upstream Precursor

CCIGHTSEKACPKY-UHFFFAOYSA-N

CC(=CCCC(C)(C=C)OC(CC1=CC=CC=C1)OC(C)(CCC=C(C)C)C2CO2)C

Environmental

Product

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

PriorBiotransformation

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

BVJSUAQZOZWCKN-UHFFFAOYSA-N

4-Hydroxybenzyl Alcohol

OCC1=CC=C(C=C1)O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

YXFVVABEGXRONW-UHFFFAOYSA-N

Toluene

C1=CC=CC=C1C

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

PriorBiotransformation

Downstream Successor

WLJVXDMOQOGPHL-UHFFFAOYSA-N

Phenylacetic Acid

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

WLJVXDMOQOGPHL-UHFFFAOYSA-N

Phenylacetic Acid

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

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

IWDCLRJOBJJRNH-UHFFFAOYSA-N

P-Cresol

c1c(ccc(c1)C)O

Precursor

RROUXOOIXJRTOM-UHFFFAOYSA-N

Linalyl phenylacetate

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

Abiotic

Downstream Successor

CFFZDZCDUFSOFZ-UHFFFAOYSA-N

Dopac

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

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

No Original Precursors

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

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.