Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H18S2 |
| Molecular Weight | 178.359 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCSSCCCC
InChI
InChIKey=CUDSBWGCGSUXDB-UHFFFAOYSA-N
InChI=1S/C8H18S2/c1-3-5-7-9-10-8-6-4-2/h3-8H2,1-2H3
| Molecular Formula | C8H18S2 |
| Molecular Weight | 178.359 |
| 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 |
|---|---|---|
| Direct observation of thiolate displacement reactions on Au(111): the role of physisorbed disulfides. | 2005-12-06 |
|
| Rhodium-catalyzed regio- and stereoselective 1-seleno-2-thiolation of 1-alkynes. | 2003-11-14 |
|
| Oxidation of sulfides and disulfides under electron transfer or singlet oxygen photosensitization using soluble or grafted sensitizers. | 2002-05 |
|
| Induction of histone acetylation in mouse erythroleukemia cells by some organosulfur compounds including allyl isothiocyanate. | 2001-06-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:55:03 GMT 2025
by
admin
on
Mon Mar 31 19:55:03 GMT 2025
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| Record UNII |
Z77EF35C0Q
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| Record Status |
Validated (UNII)
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| Record Version |
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