Search More · GCI-TPs

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

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

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

VQAREFIHUMMGEN-UHFFFAOYSA-N

4-Butyl-2-phenyl-1-[4-(phenylmethoxy)phenyl]pyrazolidine-3,5-dione

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=CC=C3)C4=CC=CC=C4

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

VQAREFIHUMMGEN-UHFFFAOYSA-N

4-Butyl-2-phenyl-1-[4-(phenylmethoxy)phenyl]pyrazolidine-3,5-dione

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=CC=C3)C4=CC=CC=C4

Environmental

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

VQAREFIHUMMGEN-UHFFFAOYSA-N

4-Butyl-2-phenyl-1-[4-(phenylmethoxy)phenyl]pyrazolidine-3,5-dione

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=CC=C3)C4=CC=CC=C4

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

VQAREFIHUMMGEN-UHFFFAOYSA-N

4-Butyl-2-phenyl-1-[4-(phenylmethoxy)phenyl]pyrazolidine-3,5-dione

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=CC=C3)C4=CC=CC=C4

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

VQAREFIHUMMGEN-UHFFFAOYSA-N

4-Butyl-2-phenyl-1-[4-(phenylmethoxy)phenyl]pyrazolidine-3,5-dione

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=CC=C3)C4=CC=CC=C4

Environmental

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

WHBNGOWSFGLIDD-UHFFFAOYSA-N

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=C(C(=C3)O)O)C4=CC=CC=C4

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

WHBNGOWSFGLIDD-UHFFFAOYSA-N

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=C(C(=C3)O)O)C4=CC=CC=C4

Environmental

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

WHBNGOWSFGLIDD-UHFFFAOYSA-N

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=C(C(=C3)O)O)C4=CC=CC=C4

Abiotic

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Upstream Precursor

WHBNGOWSFGLIDD-UHFFFAOYSA-N

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)OCC3=CC=C(C(=C3)O)O)C4=CC=CC=C4

Environmental

Product

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Environmental

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Environmental

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Environmental

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

MCRZWYDXIGCFKO-UHFFFAOYSA-N

Butylmalonic acid

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

Precursor

HFHZKZSRXITVMK-UHFFFAOYSA-N

Oxazolidin

CCCCC1C(=O)N(N(C1=O)C2=CC=C(C=C2)O)C3=CC=CC=C3

Abiotic

Downstream Successor

ZFCVUJYWMXKJJA-UHFFFAOYSA-N

4-(2-Phenylhydrazinyl)phenol

N(NC1=CC=C(C=C1)O)C2=CC=CC=C2

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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