Search More · GCI-TPs

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

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

5 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

7 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

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

WBCGRTLCAZFQHQ-UHFFFAOYSA-N

C(C(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-])Cl

Abiotic

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

WBCGRTLCAZFQHQ-UHFFFAOYSA-N

C(C(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-])Cl

Environmental

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

WBCGRTLCAZFQHQ-UHFFFAOYSA-N

C(C(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-])Cl

Environmental

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

WBCGRTLCAZFQHQ-UHFFFAOYSA-N

C(C(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-])Cl

Abiotic

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

SLOMSIRIAMJTSP-UHFFFAOYSA-N

C(C(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O…

Environmental

Product

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Previewing top 6 entries. If you want the full results, please use the download button above.

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

ICMVYBXQDUXEEE-UHFFFAOYSA-N

CID 417

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

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

GGNQRNBDZQJCCN-UHFFFAOYSA-N

1,2,4-Benzenetriol

OC1=CC(=C(C=C1)O)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

WWOBYPKUYODHDG-UHFFFAOYSA-N

4-Chlorocatechol

c1(cc(ccc1O)Cl)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

QSNSCYSYFYORTR-UHFFFAOYSA-N

4-Chloroaniline

C1=CC(=CC=C1Cl)N

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

QSNSCYSYFYORTR-UHFFFAOYSA-N

4-Chloroaniline

C1=CC(=CC=C1Cl)N

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

ITZDUMVGQACOFC-UHFFFAOYSA-N

4-Chlorobenzene-1,2,3-triol

C1(=CC=C(C(=C1O)O)Cl)O

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

HFSXRRTUWAPWSJ-UHFFFAOYSA-N

3,4-Dichlorocatechol

OC1=C(C(=CC=C1O)Cl)Cl

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

FZCQMIRJCGWWCL-UHFFFAOYSA-N

2-Amino-5-chlorophenol

C1=CC(=CC(=C1N)O)Cl

Precursor

UTZPVJKRCMYHIT-UHFFFAOYSA-N

2-(2-(4-Chloro-2-nitrophenyl)diazenyl)-N-(4-chlorophenyl)-3-oxobutanamide

CC(=O)C(C(=O)NC1=CC=C(C=C1)Cl)N=NC2=C(C=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

FZCQMIRJCGWWCL-UHFFFAOYSA-N

2-Amino-5-chlorophenol

C1=CC(=CC(=C1N)O)Cl

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.

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