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 |
|---|---|---|
| Formation of bicyclic ethers from Lewis acid promoted cyclizations of cyclic oxonium ions. | 2002 Apr 18 |
|
| Vinyl sulfide cyclized analogues of angiotensin II with high affinity and full agonist activity at the AT(1) receptor. | 2002 Apr 25 |
|
| Conformational analysis of spiro-bis-dithiepins: a peculiar case of axial chirality. | 2006 Oct 26 |
|
| Anodic coupling reactions and the synthesis of C-glycosides. | 2010 Jun 4 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:50:17 GMT 2023
by
admin
on
Fri Dec 15 19:50:17 GMT 2023
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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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-
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| Code System | Code | Type | Description | ||
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Divinyl sulfide
Created by
admin on Fri Dec 15 19:50:17 GMT 2023 , Edited by admin on Fri Dec 15 19:50:17 GMT 2023
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627-51-0
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admin on Fri Dec 15 19:50:17 GMT 2023 , Edited by admin on Fri Dec 15 19:50:17 GMT 2023
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DTXSID10211766
Created by
admin on Fri Dec 15 19:50:17 GMT 2023 , Edited by admin on Fri Dec 15 19:50:17 GMT 2023
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12321
Created by
admin on Fri Dec 15 19:50:17 GMT 2023 , Edited by admin on Fri Dec 15 19:50:17 GMT 2023
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CL87X0NVJA
Created by
admin on Fri Dec 15 19:50:17 GMT 2023 , Edited by admin on Fri Dec 15 19:50:17 GMT 2023
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PRIMARY |