Search More · GCI-TPs

Graph preview: 0 of up to 100 nodes shown.

Tab counts show list preview rows. Graph preview may show more nodes, up to 100. Export generates the full dataset subject to format and size limits.

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

8 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

9 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

17 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

18 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

18 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

17 steps

Dead-End Product

CPRDLBPDNZTCSM-UHFFFAOYSA-N

But-1-ene-1,1-diol

CCC=C(O)O

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

Upstream Precursor

DIANRASGHUFPAF-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran

CC1=CC2=C(C=C1)SCCC2

Depth 2

Product

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Upstream Precursor

DWQNSAKFPFYJHU-UHFFFAOYSA-N

6-methyl-3,4-dihydro-2H-thiochromene 1-oxide

CC1=CC2=C(C=C1)S(CCC2)=O

Depth 1

Product

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Upstream Precursor

WJHSPCJTMZROMV-UHFFFAOYSA-N

CC1=CC2=C(C=C1)[S+](CCC2)Cl

Depth 2

Product

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Previewing top 3 entries. If you want the full results, please use the download button above.

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 2

Downstream Successor

DIANRASGHUFPAF-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran

CC1=CC2=C(C=C1)SCCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 2

Downstream Successor

MDYAQVVXCCLLJP-UHFFFAOYSA-N

CC1=CC2=C(C=C1O)S(CCC2)=O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 1

Downstream Successor

DWQNSAKFPFYJHU-UHFFFAOYSA-N

6-methyl-3,4-dihydro-2H-thiochromene 1-oxide

CC1=CC2=C(C=C1)S(CCC2)=O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 2

Downstream Successor

GCWJQHOTPVLCEU-UHFFFAOYSA-N

CC1=CC2=C(C=C1)S(=O)CC(C2)O

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 1

Downstream Successor

OWAQKKRUGCCGOT-UHFFFAOYSA-N

CC1=CC2=C(C(=C1O)O)S(=O)(=O)CCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 1

Downstream Successor

NFEIKLHBORDVFK-UHFFFAOYSA-N

CC1=CC2=C(C=C1O)S(=O)(=O)CCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 3

Downstream Successor

JHUPNGKYESBYLH-UHFFFAOYSA-N

CC1=CC2=C(C=C1O)SCCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 2

Downstream Successor

WTTBUQHTPKTAJB-UHFFFAOYSA-N

CC1=CC2=C(C(=C1O)O)S(=O)CCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 3

Downstream Successor

BFAXTGOOAXQRLY-UHFFFAOYSA-N

CC1=CC2=C(C(=C1O)O)SCCC2

Precursor

WSZWAAAVGHPCNK-UHFFFAOYSA-N

3,4-Dihydro-6-methyl-2H-1-benzothiopyran 1,1-dioxide

CC1=CC2=C(C=C1)S(CCC2)(=O)=O

Depth 1

Downstream Successor

ZVBFJBKYNXMCIP-UHFFFAOYSA-N

CC1=CC2=C(C=C1)S(=O)(=O)CC(C2)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.