Search More · GCI-TPs

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

8 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

10 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

CFFZDZCDUFSOFZ-UHFFFAOYSA-N

Dopac

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Abiotic

Downstream Successor

CSEWAUGPAQPMDC-UHFFFAOYSA-N

4-Aminophenylacetic acid

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

CSEWAUGPAQPMDC-UHFFFAOYSA-N

4-Aminophenylacetic acid

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

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

PFDFJMIGPOJBQV-UHFFFAOYSA-N

3,4-Dihydroxyphenylacetamide

OC1=CC=C(C=C1O)CC(=O)N

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Abiotic

Downstream Successor

PFDFJMIGPOJBQV-UHFFFAOYSA-N

3,4-Dihydroxyphenylacetamide

OC1=CC=C(C=C1O)CC(=O)N

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Abiotic

Downstream Successor

PBFBGLBYZHLKHL-UHFFFAOYSA-N

2-(4-Aminophenyl)acetamide

C1=CC(=CC=C1CC(N)=O)N

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

PBFBGLBYZHLKHL-UHFFFAOYSA-N

2-(4-Aminophenyl)acetamide

C1=CC(=CC=C1CC(N)=O)N

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

IXDSDBYUZFMVBW-UHFFFAOYSA-N

2-(3,4-Dihydroxyphenyl)acetonitrile

Oc1c(cc(cc1)CC#N)O

Precursor

FPJRGEOLQICYQZ-UHFFFAOYSA-N

Cyclohexanecarboxamide, N-(4-(cyanomethyl)phenyl)-5-methyl-2-(1-methylethyl)-

CC1CCC(C(C1)C(=O)NC2=CC=C(C=C2)CC#N)C(C)C

Environmental

Downstream Successor

IXDSDBYUZFMVBW-UHFFFAOYSA-N

2-(3,4-Dihydroxyphenyl)acetonitrile

Oc1c(cc(cc1)CC#N)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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