Search More · GCI-TPs

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

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

9 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

8 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

10 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.

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

IQFNSSXLMQNRQZ-UHFFFAOYSA-N

2,3-Dihydroxyhexa-2,4-dienedioic acid

OC(=C(C=CC(=O)O)O)C(O)=O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

WZCZNEGTXVXAAS-UHFFFAOYSA-N

Trifluoromethanol

C(F)(F)(F)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Abiotic

Downstream Successor

WZCZNEGTXVXAAS-UHFFFAOYSA-N

Trifluoromethanol

C(F)(F)(F)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

QRBGGOMVAYBCDZ-UHFFFAOYSA-N

C(=CC(=C(O)C(=O)O)OC(F)(F)F)C(O)=O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

XQNVDQZWOBPLQZ-UHFFFAOYSA-N

p-(Trifluoromethoxy)benzaldehyde

C1=CC(=CC=C1C=O)OC(F)(F)F

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

BQHSZQCKOXTQJB-UHFFFAOYSA-N

C(=C(C(=C(O)C(=O)O)OC(F)(F)F)Cl)C(O)=O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Abiotic

Downstream Successor

NQMOGAGNCDXVDR-UHFFFAOYSA-N

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC(=C(C=C3)O)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Abiotic

Downstream Successor

NQMOGAGNCDXVDR-UHFFFAOYSA-N

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC(=C(C=C3)O)O

Precursor

RLPWBXPVBLGXBM-UHFFFAOYSA-N

1-(4-Pentylcyclohexyl)-4-[2-[4-(trifluoromethoxy)phenyl]ethynyl]benzene

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C=C3)OC(F)(F)F

Environmental

Downstream Successor

QYMSXKVDRQUNFU-UHFFFAOYSA-N

CCCCCC1CCC(CC1)C2=CC=C(C=C2)C#CC3=CC=C(C(=C3O)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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