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CAS 18293-99-7

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3,3-DIMETHYLALLYLTRIMETHYLSILANE

Description:
3,3-Dimethylallyltrimethylsilane is an organosilicon compound characterized by the presence of a trimethylsilane group attached to a 3,3-dimethylallyl moiety. This compound features a silicon atom bonded to three methyl groups and a carbon chain that includes a double bond, contributing to its reactivity and potential applications in organic synthesis and materials science. The presence of the dimethylallyl group suggests that it may participate in various chemical reactions, such as polymerization or cross-linking, making it useful in the production of silicone-based materials. Its structure indicates that it may exhibit properties typical of both silanes and alkenes, including hydrophobicity and the ability to undergo addition reactions. Additionally, the compound's volatility and low molecular weight suggest that it may be used in formulations requiring low viscosity or as a coupling agent in composite materials. Safety data should be consulted for handling and storage, as organosilicon compounds can vary in toxicity and reactivity.
Formula:C8H18Si
InChI:InChI=1/C8H18Si/c1-8(2)6-7-9(3,4)5/h6H,7H2,1-5H3
SMILES:CC(=CC[Si](C)(C)C)C
Synonyms:
  • 4-Trimethylsilyl-2-Methyl-2-Butene
  • 3-Methyl-1-Trimethylsilyl-2-Butene
  • 4-Trimethylsilyl-2-Methyl-2-Butene 97%
  • Trimethyl(3-Methyl-2-Butenyl)Silane
  • Trimethyl(3-Methylbut-2-En-1-Yl)Silane
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Found 2 products.
  • trimethyl(3-methylbut-2-en-1-yl)silane
    Indagoo
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    trimethyl(3-methylbut-2-en-1-yl)silane

    CAS:
    Formula:C8H18Si
    Molecular weight:142.314

    Ref: IN-DA0024AE

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  • Trimethyl(3-methylbut-2-en-1-yl)silane
    Biosynth
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    Trimethyl(3-methylbut-2-en-1-yl)silane

    CAS:
    Trimethyl(3-methylbut-2-en-1-yl)silane is a prenylated allyl compound. It has been shown to have antimalarial activity and can be used as a synthetic precursor in the synthesis of other allyl compounds. Trimethyl(3-methylbut-2-en-1-yl)silane is synthesized by the reaction of allyl chloride and trimethylchlorosilane, which yields high yields with stereoselective control. The reactive site of this compound is the carbon bond between the prenyl group and methyl group, which makes it useful for radical coupling reactions. Trimethyl(3-methylbut-2-en-1-yl)silane can also be used in the allylation of organic substrates, such as carbonyl groups or halides, to produce allylstannanes.
    Formula:C8H18Si
    Purity:Min. 95%
    Molecular weight:142.31 g/mol

    Ref: 3D-TAA29399

    1g
    1,003.00€