≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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
Sulfonyl fluoride motif can be used as a connector for the assembly of -SO2- linked small molecules with proteins or nucleic acids. This new click chemistry approach through sulfates is a complimentary approach to using amides and phosphate groups as linkers.
| Sonrisas canónicas | C1CC1S(=O)(=O)F |
|---|---|
| IUPAC Name | cyclopropanesulfonyl fluoride |
| InChIKey | XPOPREDCDIARJH-UHFFFAOYSA-N |
| INCHI | 1S/C3H5FO2S/c4-7(5,6)3-1-2-3/h3H,1-2H2 |
| Isómeros SMILES | C1CC1S(=O)(=O)F |
| Número ONU | 3265 |
| Peso molecular | 124.13 |
| Reaxy-Rn | 3234055 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3234055&ln= |
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 | Organohalogen compounds |
| Clase | Sulfonyl halides |
| Subclass | Sulfonyl fluorides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Sulfonyl fluorides |
| Alternative Parents | Sulfonyls Organosulfonic acids and derivatives Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Sulfonyl - Sulfonyl fluoride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as sulfonyl fluorides. These are compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a fluorine atom. |
| External Descriptors | Not available |
| Índice de refracción | n/D 1.407 |
|---|---|
| Punto de inflamación (°F) | 148.0 °F |
| Punto de inflamación (°C) | 64.44 °C |
| Peso molecular | 124.140 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 123.999 Da |
| Monoisotopic Mass | 123.999 Da |
| Topological Polar Surface Area | 42.500 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 150.000 |
| 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 |
