Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C 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.
Description
Pyridyne precursor can be activated under mild fluoride conditions; which are highly reactive with dienes and other dipolariphiles (e.g. azides) to provide cycloaddition products containing an indole motif.
| Sonrisas canónicas | C[Si](C)(C)C1=C(N=CC=C1)OS(=O)(=O)C(F)(F)F |
|---|---|
| IUPAC Name | (3-trimethylsilylpyridin-2-yl) trifluoromethanesulfonate |
| InChIKey | SXIBFUWSBRRXRJ-UHFFFAOYSA-N |
| INCHI | 1S/C9H12F3NO3SSi/c1-18(2,3)7-5-4-6-13-8(7)16-17(14,15)9(10,11)12/h4-6H,1-3H3 |
| Isómeros SMILES | C[Si](C)(C)C1=C(N=CC=C1)OS(=O)(=O)C(F)(F)F |
| WGK Alemania | 3 |
| PubChem CID | 15062470 |
| Peso molecular | 299.34 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Organic sulfonic acids and derivatives |
| Subclass | Organosulfonic acids and derivatives |
| Intermediate Tree Nodes | Alkanesulfonic acids and derivatives - Alkanesulfonic acids |
| Direct Parent | Trifluoromethanesulfonates |
| Alternative Parents | Alkylarylsilanes Organosulfonic acid esters Sulfonic acid esters Pyridines and derivatives Heteroaromatic compounds Methanesulfonates Sulfonyls Trihalomethanes Organic metalloid salts Azacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Organonitrogen compounds Organooxygen compounds Alkylsilanes |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Trifluoromethanesulfonate - Alkylarylsilane - Pyridine - Sulfonic acid ester - Organosulfonic acid ester - Methanesulfonate - Sulfonyl - Heteroaromatic compound - Trihalomethane - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Alkyl fluoride - Organosilicon compound - Alkylsilane - Hydrocarbon derivative - Halomethane - Organic oxide - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organic metalloid moeity - Organohalogen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as trifluoromethanesulfonates. These are alkanesulfonic acids, that contain a sulfonate group that is substituted with a trifluoromethyl group. |
| External Descriptors | Not available |
| Punto de inflamación (°F) | >230 °F |
|---|---|
| Punto de inflamación (°C) | >110 °C |
| Peso molecular | 299.340 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 3 |
| Exact Mass | 299.026 Da |
| Monoisotopic Mass | 299.026 Da |
| Topological Polar Surface Area | 64.599 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 385.000 |
| 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 |