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| Formula | S8 |
| Net Charge | 0 |
| Average Mass | 256.536 |
| Monoisotopic Mass | 255.77657 |
| SMILES | S1SSSSSSS1 |
| InChI | InChI=1S/S8/c1-2-4-6-8-7-5-3-1 |
| InChIKey | JLQNHALFVCURHW-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Biological Roles: | bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. fungal metabolite Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| cyclooctasulfur (CHEBI:29385) has role bacterial metabolite (CHEBI:76969) |
| cyclooctasulfur (CHEBI:29385) has role fungal metabolite (CHEBI:76946) |
| cyclooctasulfur (CHEBI:29385) is a elemental sulfur (CHEBI:33403) |
| cyclooctasulfur (CHEBI:29385) is a homomonocyclic compound (CHEBI:36913) |
| IUPAC Name |
|---|
| octathiocane |
| Synonyms | Source |
|---|---|
| S8 | IUPAC |
| cyclooctasulfur | ChemIDplus |
| octasulfur | NIST Chemistry WebBook |
| Manual Xrefs | Databases |
|---|---|
| Octasulfur | Wikipedia |
| FR2984178 | Patent |
| Registry Numbers | Sources |
|---|---|
| Gmelin:2973 | Gmelin |
| Reaxys:1099365 | Reaxys |
| CAS:10544-50-0 | ChemIDplus |
| CAS:10544-50-0 | NIST Chemistry WebBook |
| Citations |
|---|