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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-(Trimethylsilyl)-1,3-dithiane participates in Lewis base-catalyzed 1,3-dithiane addition to electrophiles such as carbonyl compounds and N-substituted aldimines. It undergoes novel diazo transfer reaction with tosyl azide in hexamethylphosphoramide-THF to yield 2-diazo-1,3-dithiane, which on decomposition yields formal carbene adducts. It is a versatile acyl anion equivalen
| Sonrisas canónicas | C[Si](C)(C)C1SCCCS1 |
|---|---|
| IUPAC Name | 1,3-dithian-2-yl(trimethyl)silane |
| InChIKey | BTTUMVHWIAXYPJ-UHFFFAOYSA-N |
| INCHI | 1S/C7H16S2Si/c1-10(2,3)7-8-5-4-6-9-7/h7H,4-6H2,1-3H3 |
| Isómeros SMILES | C[Si](C)(C)C1SCCCS1 |
| WGK Alemania | 3 |
| PubChem CID | 83413 |
| Peso molecular | 192.41 |
| Beilstein | 1616460 |
| Reaxy-Rn | 1616463 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Dithianes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dithianes |
| Alternative Parents | Trialkylsilanes Organic metalloid salts Dialkylthioethers Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | 1,3-dithiane - Trialkylsilane - Organic metalloid salt - Dialkylthioether - Thioether - Hydrocarbon derivative - Organic salt - Organosilicon compound - Alkylsilane - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dithianes. These are compounds containing a dithiane moiety, which is composed of a cyclohexane core structure wherein two methylene units are replaced by sulfur centres. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jan 17, 2026 | T162340 | |
| Certificate of Analysis | Jan 17, 2026 | T162340 | |
| Certificate of Analysis | Jan 17, 2026 | T162340 | |
| Certificate of Analysis | Jan 17, 2026 | T162340 |
| Sensibilidad | Moisture sensitive |
|---|---|
| Índice de refracción | 1.53 |
| Punto de inflamación (°F) | 204.8 °F |
| Punto de inflamación (°C) | 96°C(lit.) |
| Punto de ebullición (°C) | 77°C/2mmHg(lit.) |
| Peso molecular | 192.400 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 192.046 Da |
| Monoisotopic Mass | 192.046 Da |
| Topological Polar Surface Area | 50.600 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 103.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |