≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 Introduction
2-Chlorothioanisole can be prepared from the reaction between N,N-dimethylformamide, 1,2-dichlorobenzene, finely ground KOH and methyl mercaptan. Benzene dipole moment value analysis of 2-chlorothioanisole indicates that it exists predominantly in trans- form. 1H NMR spectrum of 2-chlorothioanisole has been studied in acetone-d6 solution.
Application
2-Chlorothioanisole may be used to synthesize 2-chlorophenyl methyl sulfone.
| Pubchem Sid | 504761368 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504761368 |
| Sorrisi canonici | CSC1=CC=CC=C1Cl |
| IUPAC Name | 1-chloro-2-methylsulfanylbenzene |
| InChIKey | IHLDFHCSSCVPQW-UHFFFAOYSA-N |
| INCHI | 1S/C7H7ClS/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3 |
| Isomeri SMILES | CSC1=CC=CC=C1Cl |
| WGK Germania | 3 |
| Peso molecolare | 158.65 |
| Beilstein | 6(4)1570 |
| Reaxy-Rn | 2042180 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2042180&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 | Organosulfur compounds |
| Classe | Thioethers |
| Subclass | Aryl thioethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aryl thioethers |
| Alternative Parents | Thiophenol ethers Chlorobenzenes Alkylarylthioethers Aryl chlorides Sulfenyl compounds Organochlorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aryl thioether - Thiophenol ether - Alkylarylthioether - Halobenzene - Chlorobenzene - Benzenoid - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Sulfenyl compound - Hydrocarbon derivative - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as aryl thioethers. These are organosulfur compounds containing a thioether group that is substituted by an aryl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 A2205086 | Certificate of Analysis | Oct 13, 2025 | C101838 |
| E2127061 | Certificate of Analysis | Mar 04, 2025 | C101838 |
| C1609013 | Certificate of Analysis | Oct 08, 2023 | C101838 |
| C2219076 | Certificate of Analysis | Feb 07, 2022 | C101838 |
| C2219133 | Certificate of Analysis | Feb 07, 2022 | C101838 |
| C2514036 | Certificate of Analysis | Feb 07, 2022 | C101838 |
| Indice di rifrazione | 1.608 |
|---|---|
| Punto di infiammabilità (°F) | 158 °F |
| Punto di infiammabilità (°C) | 70 °C |
| Punto di ebollizione (°C) | 239-240°C |
| Peso molecolare | 158.650 g/mol |
| XLogP3 | 3.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 157.996 Da |
| Monoisotopic Mass | 157.996 Da |
| Topological Polar Surface Area | 25.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 85.000 |
| 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 |
