Determine the necessary mass, volume, or concentration for preparing a solution.
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≥97% 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.
Product Application:
Thianthrene S-oxide is a sulfoxide-based thianthrene reagent for late-stage C-H functionalization.
| Sonrisas canónicas | C1=CC=C2C(=C1)SC3=CC=CC=C3S2=O |
|---|---|
| IUPAC Name | thianthrene 5-oxide |
| InChIKey | NYVGTLXTOJKHJN-UHFFFAOYSA-N |
| INCHI | 1S/C12H8OS2/c13-15-11-7-3-1-5-9(11)14-10-6-2-4-8-12(10)15/h1-8H |
| Isómeros SMILES | C1=CC=C2C(=C1)SC3=CC=CC=C3S2=O |
| PubChem CID | 73220 |
| Número NSC | NSC Number': ['16859 |
| Peso molecular | 232.32 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Benzodithiins |
| Subclass | 1,4-benzodithiins |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thianthrenes |
| Alternative Parents | Diarylthioethers Benzenoids Sulfoxides Sulfinyl compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Thianthrene - Diarylthioether - Aryl thioether - Benzenoid - Sulfoxide - Sulfinyl compound - Thioether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as thianthrenes. These are organic compounds containing a thianthrene moiety. Thianthrene is a tricyclic ring system that consists of two benzene rings fused to each other through a 1,4-dithiin ring. |
| External Descriptors | Not available |
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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 | May 19, 2026 | T588320 | |
| Certificate of Analysis | May 19, 2026 | T588320 | |
| Certificate of Analysis | May 19, 2026 | T588320 | |
| Certificate of Analysis | May 19, 2026 | T588320 |
| Sensibilidad | Air sensitive; Heat sensitive |
|---|---|
| Punto de fusión (°C) | 144 °C |
| Peso molecular | 232.300 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 232.002 Da |
| Monoisotopic Mass | 232.002 Da |
| Topological Polar Surface Area | 73.600 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 242.000 |
| 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 |