Search More · GCI-TPs

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

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

8 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

2 steps

Dead-End Product

RJZCMUPCXTXDQP-UHFFFAOYSA-N

C(=C(C(=C(O)C(=O)O)c1ccc(cc1)CCC)F)C(O)=O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

1 step

Dead-End Product

QCBGGCOCHCAEGR-UHFFFAOYSA-N

1-[4-(4-Butylcyclohexyl)phenyl]-4-(4-propylphenyl)benzene

CCCCC1CCC(CC1)c2ccc(cc2)-c3ccc(cc3)-c4ccc(cc4)CCC

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

2 steps

Dead-End Product

DECRRHWFXKPQEU-UHFFFAOYSA-N

CCCCC1CCC(CC1O)c2ccc(cc2)-c3ccc(cc3)-c4ccc(cc4)CCC

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

2 steps

Dead-End Product

MGVNJFCAPJXGCV-UHFFFAOYSA-N

CCCCC1CCC(C(C1)O)c2ccc(cc2)-c3ccc(cc3)-c4ccc(cc4)CCC

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

2 steps

Dead-End Product

NZSYLAKITYBMDT-UHFFFAOYSA-N

CCCCC1CCC(CC1)(c2ccc(cc2)-c3ccc(cc3)-c4ccc(cc4)CCC)O

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

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

GPFZQHCLHJRKOI-UHFFFAOYSA-N

CCCC(=C(C(O)=O)O)C=CC(O)=O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

GPFZQHCLHJRKOI-UHFFFAOYSA-N

CCCC(=C(C(O)=O)O)C=CC(O)=O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

UMTPHCFIYYWENL-UHFFFAOYSA-N

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

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

IMVBVLATWSHZFD-UHFFFAOYSA-N

CCCC(=C(O)C(=O)O)C(=CC(O)=O)Cl

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

MYBQQURVEVCFOW-UHFFFAOYSA-N

CCCC(=C(O)C(=O)O)C=C(Cl)C(O)=O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

PODUCNRZXJEEDO-UHFFFAOYSA-N

CCCC1=CC=C(C=C1)C(=C(O)C(=O)O)C=CC(O)=O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

PVVNQHHFXSDCKK-UHFFFAOYSA-N

CCCC(=C(O)C(=O)O)C(C(C(O)=O)O)Cl

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

CHAPLJHTPZENSI-UHFFFAOYSA-N

CCCC(C(C(O)=O)O)(C=CC(O)=O)O

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

ZQVWHZXGUYLWEX-UHFFFAOYSA-N

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

Precursor

JNNRFAYPLVJFJM-UHFFFAOYSA-N

4-[4-(4-Butylcyclohexyl)phenyl]-2-fluoro-1-(4-propylphenyl)benzene

CCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=C(C=C3)C4=CC=C(C=C4)CCC)F

Environmental

Downstream Successor

ATCXFPVBHDZYNK-UHFFFAOYSA-N

CCCC(C(C(O)=O)=O)C=CC(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.

No All Precursors

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

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