| Weight | 108.644 g/mol |
|---|---|
| Formula | C3H9ClSi |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Chlorotrimethylsilane (75-77-4)
trimethylchlorosilane
Score:
#483 in Physics
,
#1406 in Chemistry
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- Synthetic methods and reactions. 62. Transformations with chlorotrimethylsilane/sodium iodide, a convenient in situ iodotrimethylsilane reagent (Journal of Organic Chemistry, 1979)
- Modification of MCM-41 by surface silylation with trimethylchlorosilane and adsorption study (Journal of Physical Chemistry B, 1998)
- Highly selective, kinetically controlled enolate formation using lithium dialkylamides in the presence of trimethylchlorosilane (Tetrahedron Letters, 1984)
- The reactions of combined organocuprate-chlorotrimethylsilane reagents with conjugated carbonyl compounds (Tetrahedron Letters, 1985)
- Organocopper conjugate addition reaction in the presence of trimethylchlorosilane (Tetrahedron Letters, 1986)
- Conversion of ketones having , --functions to cyclopentanols by zinc-trimethylchlorosilane (Tetrahedron Letters, 1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H312: Harmful in contact with skin
Warning Acute toxicity, dermal - Category 4 - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - trimethylchlorosilane
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SMILESC[Si](C)(C)Cl
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- Pubchem - Chlorotrimethylsilane
- Wikipedia - trimethylchlorosilane
Trimethylsilyl chloride, also known as chlorotrimethylsilane is an organosilicon compound (silyl halide), with the formula (CH3)3SiCl, often abbreviated Me3SiCl or TMSCl. It is a colourless volatile liquid that is stable in the absence of water. It is widely used in organic chemistry.
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Chlorotrimethylsilane
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