Search More · GCI-TPs

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

11 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

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

NNISIBHHOUUFFS-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

NNISIBHHOUUFFS-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CBr

Environmental

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

NNISIBHHOUUFFS-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

NNISIBHHOUUFFS-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CBr

Environmental

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

NNISIBHHOUUFFS-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

SSYFNDAJKNKLRW-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CS(=O)(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Upstream Precursor

SSYFNDAJKNKLRW-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CS(=O)(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Product

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

DKGAVHZHDRPRBM-UHFFFAOYSA-N

tert-Butanol

OC(C)(C)C

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Downstream Successor

DKGAVHZHDRPRBM-UHFFFAOYSA-N

tert-Butanol

OC(C)(C)C

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Downstream Successor

WLJVXDMOQOGPHL-UHFFFAOYSA-N

Phenylacetic Acid

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

WLJVXDMOQOGPHL-UHFFFAOYSA-N

Phenylacetic Acid

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Downstream Successor

CFFZDZCDUFSOFZ-UHFFFAOYSA-N

Dopac

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

CFFZDZCDUFSOFZ-UHFFFAOYSA-N

Dopac

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Abiotic

Downstream Successor

BTVWZWFKMIUSGS-UHFFFAOYSA-N

2-Methylpropane-1,2-diol

OC(C)(C)CO

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

BTVWZWFKMIUSGS-UHFFFAOYSA-N

2-Methylpropane-1,2-diol

OC(C)(C)CO

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

LSBDFXRDZJMBSC-UHFFFAOYSA-N

Benzeneacetamide

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

Precursor

FJJNRKHLRYUGJW-UHFFFAOYSA-N

Tert-butyl 3-(bromomethyl)-5,8-dioxo-7-[(2-phenylacetyl)amino]-5lambda4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

CC(C)(C)OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CBr

Environmental

Downstream Successor

JFSQLLHRZJSJJQ-UHFFFAOYSA-N

CC(C)(C)OC(=O)C1=C(CS(=O)C2N1C(=O)C2N)CBr

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

No Original Precursors

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