Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6OS |
| Molecular Weight | 102.155 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCSC1
InChI
InChIKey=DSXFPRKPFJRPIB-UHFFFAOYSA-N
InChI=1S/C4H6OS/c5-4-1-2-6-3-4/h1-3H2
| Molecular Formula | C4H6OS |
| Molecular Weight | 102.155 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure-activity studies of cyclic ketone inhibitors of the serine protease plasmin: design, synthesis, and biological activity. | 2006-12-15 |
|
| Production of volatile organic sulfur compounds (VOSCs) by basidiomycetous yeasts. | 2005-02 |
|
| A model system study of the inhibition of heterocyclic aromatic amine formation by organosulfur compounds. | 2002-12-18 |
|
| Carbanion-induced base-catalyzed synthesis of 1H-isothiochromenes, benzo[c]thiochromenes through ring-transformation reactions of 6-aryl-2H-pyran-2-ones. | 2001-08-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:38:44 GMT 2025
by
admin
on
Mon Mar 31 19:38:44 GMT 2025
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| Record UNII |
0E9MKH53DV
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| Record Status |
Validated (UNII)
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