Search More · GCI-TPs

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

23 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.

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

NWYYWIJOWOLJNR-UHFFFAOYSA-N

Valinol

CC(C)C(CO)N

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

AXYZGMCXWZBTGT-UHFFFAOYSA-N

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

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

UYRPRYSDOVYCOU-UHFFFAOYSA-N

Benzoic acid, 2-(diphenylphosphino)-

OC(c1ccccc1P(c2ccccc2)c3ccccc3)=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

DMLVAHRVDMKGJN-UHFFFAOYSA-N

3-Diphenylphosphanylbenzene-1,2-diol

c1ccc(cc1)P(c2ccccc2)c3cccc(c3O)O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

IEHFVMWSLWDAQG-UHFFFAOYSA-N

CC(C)C1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C(=CC=CC(O)=O)C(O)=O

Precursor

OUQSAXROROGQEE-JOCHJYFZSA-N

(4S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-1,3-oxazoline

CC(C)[C@H]1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4

Environmental

Downstream Successor

VYVRWALCGRCHEM-UHFFFAOYSA-N

CC(C)C1COC(=N1)C2=CC=CC=C2P(C3=CC=CC=C3)C(C=CC(O)=O)=CC(O)=O

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.

No All Precursors

No entries were found for this section with the current query and depth.

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