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2-Chloroethanesulfonyl chloride_Molecular_structure_CAS_1622-32-8)
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2-Chloroethanesulfonyl chloride

Catalog No. A15377 Name Alfa Aesar
CAS Number 1622-32-8 Website
M. F. C2H4Cl2O2S Telephone
M. W. 163.02296 Fax
Purity 98% Email
Storage Chembase ID: 34711

SYNONYMS

Title
2-氯乙烷磺酰氯
IUPAC name
2-chloroethane-1-sulfonyl chloride
IUPAC Traditional name
2-chloroethanesulfonyl chloride
Synonyms
2-Chloroethylsulfonyl chloride

DATABASE IDS

EC Number 216-594-1
CAS Number 1622-32-8
MDL Number MFCD00007461
Beilstein Number 1751202

PROPERTIES

Purity 98%
Boiling Point 203°C
Density 1.560
Flash Point >110°C(230°F)
Refractive Index 1.4915
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Hazard statements H301-H330-H314-H318
European Hazard Symbols Highly toxic Highly toxic (T+)
GHS Precautionary statements P260-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P320-P330-P405-P501A
Risk Statements 22-26-34
RTECS KI8060000
Safety Statements 9-23-26-28-36/37/39-45
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 6.1
UN Number UN3390
Packing Group I

DETAILS

REFERENCES

  • In the presence of a base, converts alcohols to vinyl sulfonates: J. Am. Chem. Soc., 68, 1797 (1946); Angew. Chem. Int. Ed., 4, 300 (1965). These electrophilic alkenes readily undergo conjugate addition reactions with various nucleophiles:
  • Reaction with pentafluorophenol, in the presence of Et3N, gives PFP vinylsulfonate, which can be converted to a sulfonamide via tin-mediated radical addition of alkyl halides to the olefinic bond, followed by displacement of the PFP group with an amine: Org. Lett., 42549 (2002).