Search More · GCI-TPs

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

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

13 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

8 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

9 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

13 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

13 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

10 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

15 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

15 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

10 steps

Dead-End Product

ATRULDXOZAITDR-ARJAWSKDSA-N

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

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

Upstream Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

MAZFGSCCXASAEN-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2=O

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

MAZFGSCCXASAEN-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2=O

Environmental

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

MAZFGSCCXASAEN-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2=O

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

HEAVSUAZNIONPM-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2(=O)=O

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Upstream Precursor

IIPMLQVOSONXLG-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=C[S+]2Cl

Abiotic

Product

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Previewing top 8 entries. If you want the full results, please use the download button above.

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

NUJXNJXWTIQYCS-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=CC=CC=C3C)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Downstream Successor

NUJXNJXWTIQYCS-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=CC=CC=C3C)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

NUJXNJXWTIQYCS-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=CC=CC=C3C)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Downstream Successor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

YVRMQNRDXBCVAQ-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=CC(=C(C=C3C)O)O)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

CHZKNFACQALFOL-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=CC=C(C(=C3C)O)O)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Environmental

Downstream Successor

JNJDPTJPZIMPMM-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C(O)=O)C3=C(C(=CC=C3C)O)O)C=CS2

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Downstream Successor

SGPNUJHDJUWXDT-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC(=CC=C3C)O)C(C(S2)O)Cl

Precursor

SJFUUYIYTZCECB-UHFFFAOYSA-N

Benzeneacetonitrile, 2-methyl-alpha-[2-[[[(4-methylphenyl)sulfonyl]oxy]imino]-3(2H)-thienylidene]-

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=CC=C3C)C=CS2

Abiotic

Downstream Successor

WRJRYNUKTFYQFJ-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)ON=C2C(=C(C#N)C3=CC=C(C=C3C)O)C(C(S2)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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