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2,2,2-Trichloroethyl chloroformate_Molecular_structure_CAS_17341-93-4)
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2,2,2-Trichloroethyl chloroformate

Catalog No. L06875 Name Alfa Aesar
CAS Number 17341-93-4 Website
M. F. C3H2Cl4O2 Telephone
M. W. 211.85878 Fax
Purity 97% Email
Storage Chembase ID: 77889

SYNONYMS

Title
2,2,2-三氯乙基氯甲酯
IUPAC name
chloro(2,2,2-trichloroethoxy)methanone
IUPAC Traditional name
chloro(2,2,2-trichloroethoxy)methanone
Synonyms
2,2,2-Trichloroethoxycarbonyl chloride
Chloroformic acid 2,2,2-trichloroethyl ester

DATABASE IDS

MDL Number MFCD00000810
CAS Number 17341-93-4
Beilstein Number 970619
EC Number 241-363-7

PROPERTIES

Purity 97%
Boiling Point 171-172°C
Density 1.539
Flash Point >100°C(212°F)
Melting Point 0-2°C
Refractive Index 1.4700
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Hazard statements H301-H330-H314-H318
European Hazard Symbols Toxic Toxic (T)
GHS Precautionary statements P260-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P320-P330-P405-P501A
Risk Statements 22-23-34
Safety Statements 9-20-26-36/37/39-45
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 6.1
UN Number UN3277
Packing Group II

DETAILS

REFERENCES

  • Reagent for the protection of OH groups as their trichloroethyl (Troc) carbonates, specifically cleaved by reduction with zinc: Tetrahedron Lett., 2555 (1967). For a systematic study of the protection of amines as their Troc-carbamates, see: Synthesis, 268 (1981).
  • Preferred to ethyl chloroformate for the N-demethylation of tert-amines, since the resulting carbamate can be cleaved by reductive elimination: Tetrahedron Lett., 1325 (1974); Synth. Commun., 7, 79 (1977).
  • Effective reagent for dehydration of primary amides to nitriles: Synth. Commun., 30, 3047 (2000).
  • For a brief survey of uses of this reagent in synthesis, see: Synlett, 1473 (2007).