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Methoxyacetyl chloride_Molecular_structure_CAS_38870-89-2)
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Methoxyacetyl chloride

Catalog No. L03210 Name Alfa Aesar
CAS Number 38870-89-2 Website
M. F. C3H5ClO2 Telephone
M. W. 108.5236 Fax
Purity 97%, stab. with ca 0.3% magnesium oxide Email
Storage Chembase ID: 88363

SYNONYMS

Title
甲氧基乙酰氯
IUPAC name
2-methoxyacetyl chloride
IUPAC Traditional name
methoxy-acetyl chloride

DATABASE IDS

MDL Number MFCD00000728
CAS Number 38870-89-2
EC Number 254-169-2
Beilstein Number 1740244

PROPERTIES

Purity 97%, stab. with ca 0.3% magnesium oxide
Boiling Point 112-113°C
Density 1.185
Flash Point 28°C(82°F)
Melting Point <-40°C
Refractive Index 1.4240
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Hazard statements H331-H314-H318-H226
European Hazard Symbols X
European Hazard Symbols Corrosive Corrosive (C)
GHS Precautionary statements P280-P305+P351+P338-P309-P310
Risk Statements 10-20-34
Safety Statements 26-36/37/39-45
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 8
UN Number UN2920
Packing Group II

DETAILS

REFERENCES

  • Reagent for the chloromethylation of aromatics under Friedel-Crafts conditions, avoiding the use of chloromethyl methyl ether: Tetrahedron Lett., 24, 1933 (1983). For a study of the kinetics of chloromethylation of benzene and toluene in the presence of SnCl4, see: J. Org. Chem., 62, 2694 (1997). Compare Methoxyacetic acid, B22917.
  • Has also been used for the protection of alcohols as methoxyacetate esters, formed in the presence of pyridine, and cleaved using methanolic or aqueous ammonia ca. 20x faster than acetate: Tetrahedron Lett., 4273 (1968). Selective cleavage with Yb(OTf)3: J. Org. Chem., 61, 4491 (1996), or ethanolamine in IPA: J. Org. Chem., 60, 331 (1995), have also been reported.