Chloromethyl Methyl Sulfide - ≥97%(GC) , CAS No.2373-51-5

CAS: 2373-51-5 Cat. No.: C153265 Molecular Weight: 96.57 Beilstein Registry Number: 1730850 EC Number: 219-148-4

GRADE & PURITY ≥97%(GC)

Synonyms

NSC63205 | NSC-63205 | chloro-(methylthio)methane | Chloromethylmethyl sulfide | Chlorodimethyl sulfide | chloromethyl methylsulfide | Methylthiomethyl chloride | STR09358 | (Chloromethyl) methyl sulfide | chloromethyl methylthioether | chloromethylmethyl

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

NSC63205 | NSC-63205 | chloro-(methylthio)methane | Chloromethylmethyl sulfide | Chlorodimethyl sulfide | chloromethyl methylsulfide | Methylthiomethyl chloride | STR09358 | (Chloromethyl) methyl sulfide | chloromethyl methylthioether | chloromethylmethyl

Specifications & Purity

≥97%(GC)

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%(GC)

Names and Identifiers

• Canonical Smiles: CSCCl
• IUPAC Name: chloro(methylsulfanyl)methane
• InChIKey: JWMLCCRPDOIBAV-UHFFFAOYSA-N
• INCHI: 1S/C2H5ClS/c1-4-2-3/h2H2,1H3
• Isomeric SMILES: CSCCl
• WGK Germany: 3
• RTECS: WQ3700000
• Molecular Weight: 96.57
• Beilstein: 1730850
• Reaxy-Rn: 1730851
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1730851&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Class Thioethers
      • Subclass Dialkylthioethers

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Class: Thioethers
• Subclass: Dialkylthioethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkylthioethers
• Alternative Parents: Sulfenyl compounds Organochlorides Hydrocarbon derivatives Alkyl chlorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Air Sensitive;Heat Sensitive;Moisture sensitive
• Refractive Index: 1.5
• Flash Point(°F): 62.6 °F
• Flash Point(°C): 17°C(lit.)
• Boil Point(°C): 106°C
• Molecular Weight: 96.580 g/mol
• XLogP3: 1.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 95.98 Da
• Monoisotopic Mass: 95.98 Da
• Topological Polar Surface Area: 25.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.000
• 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

References

1. Jin Li, Junjie Chen, Xiaosa Xu, Zhenyu Wang, Zixiao Guo, Pengzhu Lin, Jing Sun, Baoling Huang, Tianshou Zhao.  (2025)  Electrolyte/electrode interphase regulation with methylthiolation ionic liquids for high-voltage quasi–solid-state Li metal batteries.  Science Advances,  11  (46):   [PMID:41237230] [10.1126/sciadv.adz5203]