Determine the necessary mass, volume, or concentration for preparing a solution.
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Storage
Room temperature
| ALogP | 0.6 |
|---|
| Canonical Smiles | CSCC1CO1 |
|---|---|
| IUPAC Name | 2-(methylsulfanylmethyl)oxirane |
| InChIKey | OSIXFNQHNPOVIA-UHFFFAOYSA-N |
| INCHI | 1S/C4H8OS/c1-6-3-4-2-5-4/h4H,2-3H2,1H3 |
| Isomeric SMILES | CSCC1CO1 |
| PubChem CID | 548390 |
| Molecular Weight | 104.17 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Epoxides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Epoxides |
| Alternative Parents | Sulfenyl compounds Oxacyclic compounds Dialkylthioethers Dialkyl ethers Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Oxacycle - Dialkylthioether - Sulfenyl compound - Thioether - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms). |
| External Descriptors | Not available |
| Molecular Weight | 104.170 g/mol |
|---|---|
| XLogP3 | 0.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 104.03 Da |
| Monoisotopic Mass | 104.03 Da |
| Topological Polar Surface Area | 37.800 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 46.800 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |