| Weight | 150.725 g/mol |
|---|---|
| Formula | C6H15ClSi |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Tert-Butyldimethylsilyl chloride (18162-48-6)
t-butyldimethylchlorosilane · t-butyldimethylchlorsilane · TBMCS cpd
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- Reaction of tert-butyldimethylsilyl esters with oxalyl chloride-dimethylformamide: preparation of carboxylic acid chlorides under neutral conditions (Journal of Organic Chemistry, 1978)
- Use of t-butyldimethylchlorosilane/imidazole reagent for identification of molecular species of phospholipids by gas-liquid chromatography mass spectrometry. (Journal of Mass Spectrometry, 1979)
- Cleavage of tert-butyldimethylsilyl ethers by chloride ion (Tetrahedron Letters, 1998)
- Palladium-catalyzed heteroarylation of 1-(tert-butyldimethylsilyl)-3-indolylzinc chloride. Efficient synthesis of 3-(2-pyridyl)indoles (Tetrahedron Letters, 1994)
- A Catalytic Amount of Nickel(II) Chloride Hexahydrate and 1,2-Ethanedithiol is a Good Combination for the Cleavage of Tetrahydropyranyl (THP) and tert-Butyldimethylsilyl (TBS) Ethers. (Tetrahedron Letters, 2005)
- A mild and selective cleavage of tert-butyldimethylsilyl ethers by indium(III) chloride (New Journal of Chemistry, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - t-butyldimethylchlorosilane
- t-butyldimethylchlorsilane
- TBMCS cpd
-
SMILESCC(C)(C)[Si](C)(C)Cl
-
InChIKeyBCNZYOJHNLTNEZ-UHFFFAOYSA-N
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