Search More · GCI-TPs

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

8 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

15 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

29 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

29 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

16 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

IUGYQRQAERSCNH-UHFFFAOYSA-N

Pivalic acid

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

QHPQWRBYOIRBIT-UHFFFAOYSA-N

4-tert-Butylphenol

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

QHPQWRBYOIRBIT-UHFFFAOYSA-N

4-tert-Butylphenol

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

WQZUKHHOYITOFD-UHFFFAOYSA-N

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

WQZUKHHOYITOFD-UHFFFAOYSA-N

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

XESZUVZBAMCAEJ-UHFFFAOYSA-N

4-tert-Butylcatechol

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

ODFOJAXEKVBHQS-UHFFFAOYSA-N

p-tert.-Butylphenol-dialkohol

CC(C)(C)c1ccc(c(c1O)O)O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

HLCMVIMBGDVDHH-UHFFFAOYSA-N

3-Tert-butylhexa-2,4-dienedioic acid

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

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

NMZURFAPYNEBQQ-UHFFFAOYSA-N

Phenol, 4-(1,1-dimethylethyl)-, 1,1'-(hydrogen phosphate)

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)O

Precursor

PFWJBHJSKGMFNK-UHFFFAOYSA-N

Phosphorochloridic acid, bis[4-(1,1-dimethylethyl)phenyl] ester

CC(C)(C)C1=CC=C(C=C1)OP(=O)(OC2=CC=C(C=C2)C(C)(C)C)Cl

Environmental

Downstream Successor

PRLINSMUYJWPBL-UHFFFAOYSA-N

4-tert-Butyl-2-chlorophenol

CC(C)(C)c1ccc(c(c1)Cl)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.