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About This Item
Linear Formula:
(CH3)3CSiCl3
CAS Number:
Molecular Weight:
191.56
Beilstein:
1736174
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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Assay
96%
form
solid
bp
132-134 °C (lit.)
mp
97-100 °C (lit.)
SMILES string
CC(C)(C)[Si](Cl)(Cl)Cl
InChI
1S/C4H9Cl3Si/c1-4(2,3)8(5,6)7/h1-3H3
InChI key
MOOUPSHQAMJMSL-UHFFFAOYSA-N
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General description
tert-Butyltrichlorosilane is a tert-alkyltrichlorosilane that can be prepared by reacting trimethyl chloride and silicon tetrachloride. It can be used in the synthesis of tert-butyl silsequioxanes by hydrolytic condensation in DMSO.
Application
Hydrolytic condensation of tert-butyltrichlorosilane (tBuSiCl3)in DMSO and water was investigated. The process results in the formation of tBu2Si2O(OH)4, the Ti complex of the intermediate produce active heterogeneous epoxidation catalysts.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Sol. 1 - Skin Corr. 1B
Supplementary Hazards
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
104.0 °F - closed cup
Flash Point(C)
40 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Silsesquioxane-Based Homogeneous and Heterogeneous Epoxidation Catalysts Developed by Using High-Speed Experimentation
Pescarmona PP, et al.
Chemistry?A European Journal , 10(7), 1657-1665 (2004)
Silsesquioxane-Based Homogeneous and Heterogeneous Epoxidation Catalysts Developed by Using High-Speed Experimentation,
Pescarmona PP, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 116 (38), 20433-20437 (2012)
Organomagnesium synthesis of sec-butyl-and tert-alkylchlorogermanes and their reaction with ethynylmagnesium bromide
Yarosh OG, et al.
Russ. J. Gen. Chem., 75(5), 714-718 (2005)
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