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(Chloromethyl)trimethylsilane

Catalog No. A14303 Name Alfa Aesar
CAS Number 2344-80-1 Website
M. F. C4H11ClSi Telephone
M. W. 122.66864 Fax
Purity 98% Email
Storage Chembase ID: 87753

SYNONYMS

Title
(氯甲基)三甲基硅烷
IUPAC name
(chloromethyl)trimethylsilane
IUPAC Traditional name
(chloromethyl)trimethylsilane

DATABASE IDS

EC Number 219-058-5
CAS Number 2344-80-1
MDL Number MFCD00000878
Beilstein Number 906705

PROPERTIES

Purity 98%
Boiling Point 97-98°C
Density 0.886
Flash Point -2°C(28°F)
Refractive Index 1.4180
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Hazard statements H224-H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
European Hazard Symbols Flammable Flammable (F)
GHS Precautionary statements P210-P241-P303+P361+P353-P305+P351+P338-P405-P501A
Risk Statements 11-36/37/38
Safety Statements 9-16-23-26-33-37
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 3
UN Number UN1993
Packing Group II

DETAILS

REFERENCES

  • For a review of the chemistry of chloromethyltrimethylsilane, see: Synthesis, 717 (1985).
  • Treatment with s-BuLi at -78o gives ɑ-lithio-ɑ-chloromethyltrimethylsilane which reacts with aldehydes and ketones to give ɑ?-epoxy silanes, readily hydrolyzed to homologated aldehydes: Tetrahedron, 39, 867 (1983):
  • Metallation gives useful precursors of various organosilicon compounds. For use of the Grignard in the olefination of ketones, see: J. Org. Chem., 39, 3264 (1974); 52, 281 (1987). For Ni-catalyzed reaction of the Grignard with allylic dithioacetals, see: J. Org. Chem., 53, 5582 (1988); Org. Synth. Coll., 9, 727 (1998); for an example with reaction scheme, see trans-Cinnamaldehyde, A14689.