AC-18749 - iodotrimethylsilane-95-97-stabilized | 16029-98-4

Iodotrimethylsilane is used for the introduction of trimethylsilyl group in organic synthesis. It is also useful for gas chromatography analysis by converting alcohol into a silyl ether derivative, thereby making it more volatile than the original molecule. This Thermo Scientific Chemicals brand pro

S19550 - Trimethylsilyl iodide (stabilised with 0.1% Copper)

Stability Moisture Sensitive (Reactive)
Applications Iodotrimethylsilane is a reagent used for cleaving ethers, esters, carbamates, ketals and lactones.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Heck, M., et al.: Tetrahedron Lett., 35, 5445 (1994); Hiral, G., et al.: Biorg. Med. Chem. Lett., 14, 2647 (2004)

Trimethylsilyl Blocking Agent
Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.
Trimethyliodosilane; Iodotrimethylsilane, Trimethylsilyl iodide; TMIS
Extremely reactive silylating agentUsed with HMDS for hindered alcoholsForms enol silyl ethers with ketones and SIT8620.0Nafion SAC-13 has been shown to be a recyclable catalyst for the trimethylsilylation of primary, secondary, and tertiary alcohols in excellent yields and short reaction timesSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Iodotrimethylsilane is an organic compound with the chemical formula CH3I. It is a colorless liquid that reacts with hydroxyl groups to produce iodide. Iodotrimethylsilane can be used in sample preparation for biological samples and organic chemists use it as a model system for reactions involving iodination reactions. Iodotrimethylsilane is prepared by the reaction of sodium metal in anhydrous sodium trifluoroacetate with trimethoxysilane, which produces sodium iodide and trimethoxysilane: