Search More · GCI-TPs

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

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

8 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.

Upstream Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Product

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Upstream Precursor

KTXTUWJHPLDBSO-UHFFFAOYSA-N

CCOC(=O)C1=CC=C(C=C1)N=C[N+](CC2=CC=CC=C2)(C3=CC=C(C=C3)C(=O)…

Environmental

Product

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

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

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

WHRPFDOAMQIPQF-UHFFFAOYSA-O

Benzyl-[(4-ethoxycarbonylanilino)methylidene]-(4-ethoxycarbonylphenyl)azanium

CCOC(=O)C1=CC=C(C=C1)N=C[NH+](CC2=CC=CC=C2)C3=CC=C(C=C3)C(=O)OCC

Abiotic

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

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

No Original Precursors

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