Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6S |
| Molecular Weight | 86.155 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CSC=C
InChI
InChIKey=UIYCHXAGWOYNNA-UHFFFAOYSA-N
InChI=1S/C4H6S/c1-3-5-4-2/h3-4H,1-2H2
| Molecular Formula | C4H6S |
| Molecular Weight | 86.155 |
| 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 |
|---|---|---|
| Anodic coupling reactions and the synthesis of C-glycosides. | 2010-06-04 |
|
| Intramolecular anodic olefin coupling reactions: using competition studies to probe the mechanism of oxidative cyclization reactions. | 2010-04-16 |
|
| Electron-deficient alkynes as cleavable reagents for the modification of cysteine-containing peptides in aqueous medium. | 2009 |
|
| Reactions at the Ru-S bonds of coordinatively unsaturated ruthenium complexes with tethered 2,6-dimesitylphenyl thiolate. | 2008-09-01 |
|
| Conformational analysis of spiro-bis-dithiepins: a peculiar case of axial chirality. | 2006-10-26 |
|
| Analogs of squalene and oxidosqualene inhibit oxidosqualene cyclase of Trypanosoma cruzi expressed in Saccharomyces cerevisiae. | 2005-12 |
|
| The reactions of sulfur mustard with the active components of organic decontaminants. | 2005-08-31 |
|
| Vinyl sulfide cyclized analogues of angiotensin II with high affinity and full agonist activity at the AT(1) receptor. | 2002-04-25 |
|
| Formation of bicyclic ethers from Lewis acid promoted cyclizations of cyclic oxonium ions. | 2002-04-18 |
|
| Vinyl sulfide derivatives of truncated oxidosqualene as selective inhibitors of oxidosqualene and squalene-hopene cyclases. | 2001-06 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:58:15 GMT 2025
by
admin
on
Mon Mar 31 19:58:15 GMT 2025
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| Record UNII |
CL87X0NVJA
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| Record Status |
Validated (UNII)
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| Record Version |
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Divinyl sulfide
Created by
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627-51-0
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DTXSID10211766
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12321
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CL87X0NVJA
Created by
admin on Mon Mar 31 19:58:15 GMT 2025 , Edited by admin on Mon Mar 31 19:58:15 GMT 2025
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PRIMARY |