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1-Chloro-1-methylsilacyclobutane / 5 G

Purity: 98 %
Synonym: 1-Chloro-1-methylsiletane; cyclotrimethylenemethylchlorosilane
Molecular Formula: C4H9ClSi
Molecular Weight: 120.65
SKU: MND-61662
CAS Number: 2351-34-0
MDL number: MFCD00191926
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 G  
182.70 EUR



Safety Information


Hazard Statements

H225
H314

Precautionary Statements

P210
P280
P303 + P361 + P353
P305 + P351 + P338
P233
P240

Pictograms



Properties

Signal WordDanger
Flash Point (C)3 °C - closed cup
Flash Point (F)37.4 °F - closed cup
Density0.985 g/mL at 25 °C (lit.)
Boiling Point103 °C (lit.)

 Product Description

"1-CHLORO-1-METHYLSILACYCLOBUTANE is a chemical compound used in organic synthesis for the preparation of various silicon-containing molecules. It serves as a valuable reagent in the creation of silicon-based intermediates and compounds."

 

Application:

"Applied in organic synthesis, 1-CHLORO-1-METHYLSILACYCLOBUTANE functions as a crucial reagent for the generation of silicon-containing intermediates, playing a significant role in the development of diverse chemical compounds."

 

 

Articles:

- Raman and infrared spectra, conformational stability, normal coordinate analysis, ab initio calculations and vibrational assignment of 1-chloro-1-methylsilacyclobutane

Publication Date: 10 May 1999

Todor K. Gounev, Gamil A. Guirgis, Tarek A. Mohamed, Pengqian Zhen, James R. Durig

https://doi.org/10.1002/(SICI)1097-4555(199905)30:5<399::AID-JRS382>3.0.CO;2-F

 

- Infrared, and Raman spectra, conformational stability, normal coordinate analysis, ab initio calculations, and vibrational assignment of 1-chlorosilacyclobutane

Publication Date: Available online 6 June 2000

J.R. Durig, T.K. Gounev, P. Zhen, G.A. Guirgis

https://doi.org/10.1016/S0166-1280(00)00381-X

 

- An improved cyclization procedure for 3-chloropropylchlorosilanes: Efficient syntheses of silacyclobutanes

Publication Date: Available online 4 June 2001

R. Damrauer, R.A. Davis, M.T. Burke, R.A. Karn, G.T. Goodman

https://doi.org/10.1016/S0022-328X(00)81771-4