Determine the necessary mass, volume, or concentration for preparing a solution.
≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light 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
Mechanism of formation of trimethylene oxide from 3-chloropropyl thiolacetate has been investigated.
| Sonrisas canónicas | CC(=O)SCCCCl |
|---|---|
| IUPAC Name | S-(3-chloropropyl) ethanethioate |
| InChIKey | IOLUCUQNAZTKMN-UHFFFAOYSA-N |
| INCHI | 1S/C5H9ClOS/c1-5(7)8-4-2-3-6/h2-4H2,1H3 |
| Isómeros SMILES | CC(=O)SCCCCl |
| WGK Alemania | 3 |
| Peso molecular | 152.64 |
| Reaxy-Rn | 1745347 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1745347&ln= |
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 | Thiocarboxylic acids and derivatives |
| Subclass | Thioesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thioesters |
| Alternative Parents | Carbothioic S-esters Sulfenyl compounds Carboxylic acids and derivatives Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbothioic s-ester - Thiocarboxylic acid ester - Sulfenyl compound - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as thioesters. These are organic compounds containing an ester of thiocarboxylic acid, with the general structure RC(=S)XR' (R=H, alkyl, aryl; R'=alkyl, aryl; X=O,S). |
| External Descriptors | Not available |
| Sensibilidad | light & Moisture sensitive |
|---|---|
| Punto de inflamación (°F) | 172.4 °F |
| Punto de inflamación (°C) | 78 °C |
| Peso molecular | 152.640 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | 152.006 Da |
| Monoisotopic Mass | 152.006 Da |
| Topological Polar Surface Area | 42.400 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 74.800 |
| 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 |