Difluoromethanesulfonyl chloride - ≥96% , CAS No.1512-30-7

CAS: 1512-30-7 Cat. No.: D181664 Molecular Weight: 150.5 EC Number: 216-150-7

GRADE & PURITY ≥96%

Synonyms

difluoromethanesulfonyl chloride|1512-30-7|Difluoromethanesulphonyl chloride|Methanesulfonylchloride, 1,1-difluoro-|MFCD09971548|difluoromethylsulfonyl chloride|Methanesulfonyl chloride, difluoro-|EINECS 216-150-7|HCF2SO2Cl|SCHEMBL916367|difluoro-methanes

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

application：

Difluoromethanesulfonyl Chloride is a reactant used in the synthesis of ketoconazole sulfonamide analogs as antifungal agents.

Specifications

Synonyms

difluoromethanesulfonyl chloride | 1512-30-7 | Difluoromethanesulphonyl chloride | Methanesulfonylchloride, 1, 1-difluoro- | MFCD09971548 | difluoromethylsulfonyl chloride | Methanesulfonyl chloride, difluoro- | EINECS 216-150-7 | HCF2SO2Cl | SCHEMBL916367 | difluoro-methanes

Specifications & Purity

≥96%

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

≥96%

Names and Identifiers

• Canonical Smiles: C(F)(F)S(=O)(=O)Cl
• IUPAC Name: difluoromethanesulfonyl chloride
• InChIKey: JYQLKKNUGGVARY-UHFFFAOYSA-N
• INCHI: 1S/CHClF2O2S/c2-7(5,6)1(3)4/h1H
• Isomeric SMILES: C(F)(F)S(=O)(=O)Cl
• Molecular Weight: 150.5
• Reaxy-Rn: 2350249
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2350249&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Class Sulfonyl halides
      • Subclass Sulfonyl chlorides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Class: Sulfonyl halides
• Subclass: Sulfonyl chlorides
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfonyl chlorides
• Alternative Parents: Sulfonyls Organosulfonic acids and derivatives Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sulfonyl - Sulfonyl chloride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organofluoride - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sulfonyl chlorides. These are compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a chlorine atom.
• 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

• Solubility: Solubility in Chloroform
• Sensitivity: Moisture sensitive
• Flash Point(°C): 5 °C
• Boil Point(°C): 95-99℃
• Molecular Weight: 150.530 g/mol
• XLogP3: 1.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 149.935 Da
• Monoisotopic Mass: 149.935 Da
• Topological Polar Surface Area: 42.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 132.000
• 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