Weight | 192.806 g/mol |
---|---|
Formula | C9H21ClSi |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Triisopropylsilyl chloride (13154-24-0)
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LabBot
- Efficient and Selective Protection of Alcohols and Phenols with Triisopropylsilyl Chloride/Imidazole Using Microwave Irradiation (Tetrahedron, 2000)
- EFFECTIVE SILYLATION OF CARBOXYLIC ACIDS UNDER SOLVENT-FREE CONDITIONS WITH tert-BUTYLDIMETHYLSILYL CHLORIDE (TBDMSCL) AND TRIISOPROPYLSILYL CHLORIDE (TIPSCL) (Phosphorus Sulfur and Silicon and The Related Elements, 2000)
- 724. Nucleophilic substitution reactions of organosilicon compounds. Part I. Reactions of triisopropylsilyl chloride (Journal of The Chemical Society (resumed), 1957)
- ChemInform Abstract: Efficient and Selective Protection of Alcohols and Phenols with Triisopropylsilyl Chloride/Imidazole Using Microwave Irradiation. (ChemInform, 2001)
- Efficient and Practical Procedure for the Esterification of the Free -Carboxylic Acid of Amino Acid Residues with -(Trimethylsilyl)ethoxymethyl Chloride and Triisopropylsilyl Chloride (Synthesis, 2014)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)[Si](C(C)C)(C(C)C)Cl
-
InChIKeyKQIADDMXRMTWHZ-UHFFFAOYSA-N
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