| Weight | 188.389 g/mol |
|---|---|
| Formula | C2H4S5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,2,3,5,6-Pentathiepane (292-46-6)
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- Sigma-Aldrich - Search for 1,2,3,5,6-Pentathiepane
- Fisher Scientific - Search for 1,2,3,5,6-Pentathiepane
- TCI - Search for 1,2,3,5,6-Pentathiepane
- Reaction of a stable germabenzene with chalcogens: synthesis and structure of a novel germanium analog of pentathiepane, 1,2,3,4,5,6-pentathiagermepane (Journal of Organometallic Chemistry, 2003)
- The Synthesis of 4,4,7,7-Tetrabenzyl-1,2,3,5,6-pentathiepane. (Acta Chemica Scandinavica, 1959)
- Determination of 1,2,3,5,6-Pentathiepane in Lentinula edodes by Gas Chromatography-Mass Spectrometry (Food Science, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1SSCSSS1
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InChIKeyDZKOKXZNCDGVRY-UHFFFAOYSA-N
- Pubchem - 1,2,3,5,6-Pentathiepane
- Wikipedia - lenthionine
Lenthionine is a cyclic organosulfur compound found in shiitake mushrooms and partly responsible for their flavor. The mechanism of its formation is unclear, but it probably involves the enzyme CS lyase. Besides giving flavor to shiitake mushrooms, lenthionine inhibits platelet aggregation, so it is a promising treatment for thrombosis.
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1,2,3,5,6-Pentathiepane
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