CAS 16029-98-4
:Silane, iodotrimethyl-
Description:
Silane, iodotrimethyl- is an organosilicon compound characterized by the presence of a silicon atom bonded to three methyl groups and one iodine atom. Its molecular structure can be represented as Si(CH₃)₃I, indicating that the silicon is tetravalent, forming four covalent bonds. This compound is typically a colorless to pale yellow liquid with a relatively low boiling point, making it volatile. It is known for its reactivity, particularly in nucleophilic substitution reactions due to the presence of the iodine atom, which can be replaced by other nucleophiles. Silane, iodotrimethyl- is often used in organic synthesis and as a reagent in various chemical reactions, including those involving silicon-based materials. Additionally, it may exhibit properties such as flammability and potential toxicity, necessitating careful handling and storage. Its applications can extend to the fields of materials science and surface modification, where it can act as a coupling agent or a precursor for silicon-containing compounds.
Formula:C3H9ISi
InChI:InChI=1/C3H9ISi/c1-5(2,3)4/h1-3H3
InChI key:InChIKey=CSRZQMIRAZTJOY-UHFFFAOYSA-N
SMILES:[Si](C)(C)(C)I
Synonyms:- Iodotrimethylsilan
- Iodotrimethylsilane
- Iodotrimetilsilano
- Trimethyliodosilane
- Trimethylsilicon iodide
- Trimethylsilyl iodide
- Trimethyliodosilanestabilizedwithcoppergranules
- Silane, iodotrimethyl-
- Tri methyl silyl iodide
- Trimethyl iodosilane
- Iodotrmethylsilane
- TMS iodide
- TMIS
- Iodotrimethylsilane, stabilised with copper, 95%
- trimethyliodosilane(tmis)
- iodotrimethyl-silan
- IODOTRIMETHYLSILANE, STAB.
- IODO TRIMETHYL SILYL
- Iodotrimethylsilane, 97%, stab. with copper
- CT3610
- IODOTRIMETHYLSILANE , STABILIZED WITH COPPER
- Trimethylsilysiodide
- Iodotrimethylsilane, stabilized, 95-97%
- IODOTRIMETHYLSILYL IODIDE
- See more synonyms
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Found 9 products.
Trimethylsilyl Iodide (stabilized with Aluminum)
CAS:Formula:C3H9ISiPurity:>95.0%(T)Color and Shape:Colorless to Brown clear liquidMolecular weight:200.09Iodotrimethylsilane, 97%, stab. with copper
CAS:<p>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</p>Formula:C3H9ISiPurity:97%Color and Shape:Clear colorless to red or brown, LiquidMolecular weight:200.09Iodotrimethylsilane
CAS:<p>Iodotrimethylsilane</p>Formula:C3H9ISiPurity:≥95%Color and Shape: clear. very dark red/brown liquidMolecular weight:200.09g/molTrimethylsilyl iodide (stabilised with 0.1% Copper)
CAS:<p>S19550 - Trimethylsilyl iodide (stabilised with 0.1% Copper)</p>Formula:C3H9ISiPurity:98%Color and Shape:Liquid, Clear LiquidMolecular weight:200.094Iodotrimethylsilane (>90%)
CAS:<p>Stability Moisture Sensitive (Reactive)<br>Applications Iodotrimethylsilane is a reagent used for cleaving ethers, esters, carbamates, ketals and lactones.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Heck, M., et al.: Tetrahedron Lett., 35, 5445 (1994); Hiral, G., et al.: Biorg. Med. Chem. Lett., 14, 2647 (2004)<br></p>Formula:C3H9ISiPurity:>90%Color and Shape:NeatMolecular weight:200.09Iodotrimethylsilane
CAS:<p>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:</p>Formula:C3H9ISiPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:200.09 g/molTRIMETHYLIODOSILANE
CAS:<p>Trimethylsilyl Blocking Agent<br>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.<br>Trimethyliodosilane; Iodotrimethylsilane, Trimethylsilyl iodide; TMIS<br>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<br></p>Formula:C3H9ISiPurity:97%Color and Shape:Straw To Pale Pink-Purple LiquidMolecular weight:200.1








