Search More · GCI-TPs

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

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(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

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

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

SJAQFWWPZHJRPU-UHFFFAOYSA-N

2-Chloro-N-(2-(hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOC1=C(C=C(C=C1)S(=O)(=O)NC)NC(=O)C(C(=O)C(C)(C)C)Cl

Abiotic

Product

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Upstream Precursor

SJAQFWWPZHJRPU-UHFFFAOYSA-N

2-Chloro-N-(2-(hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOC1=C(C=C(C=C1)S(=O)(=O)NC)NC(=O)C(C(=O)C(C)(C)C)Cl

Environmental

Product

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

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

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Abiotic

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

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

Precursor

CCXDKYUOXACLTK-UHFFFAOYSA-N

N-(2-(Hexadecyloxy)-5-((methylamino)sulphonyl)phenyl)-4,4-dimethyl-3-oxovaleramide

CCCCCCCCCCCCCCCCOc1c(cc(cc1)S(=O)(=O)NC)NC(=O)CC(=O)C(C)(C)C

Environmental

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

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

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

No Original Precursors

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