762-72-1
Chemical Structure
Allyltrimethylsilane
Synonym(s): Trimethyl-prop-2-enylsilane
- CAS No.: 762-72-1
- Formula:C6H14Si
- Molecular Weight:114.26
IUPAC Name: allyltrimethylsilane
InChIKey: HYWCXWRMUZYRPH-UHFFFAOYSA-N
SMILES: C[Si](C)(C)CC=C
Biological Activity: Allyltrimethylsilane (Trimethyl-prop-2-enylsilane) is an organosilicon compound. Allyltrimethylsilane undergoes photochemical thiol-ene reactions with thiolated soybean oil. Allyltrimethylsilane participates in carbon-carbon bond formation via allylation reactions with acetals, ketals, aldehydes and ketones, forms cyclopropane through reaction with aldehydes, and reacts with iodine to produce trimethylsilyl iodide. Allyltrimethylsilane is applicable to research related to organic synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Allyltrimethylsilane | 99.57% | Allyltrimethylsilane (Trimethyl-prop-2-enylsilane) is an organosilicon compound. Allyltrimethylsilane undergoes photochemical thiol-ene reactions with thiolated soybean oil. Allyltrimethylsilane participates in carbon-carbon bond formation via allylation reactions with acetals, ketals, aldehydes and ketones, forms cyclopropane through reaction with aldehydes, and reacts with iodine to produce trimethylsilyl iodide. Allyltrimethylsilane is applicable to research related to organic synthesis. | ||||||||||||||||||||
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- [1]. Ionescu M, et al. Functionalized vegetable oils as precursors for polymers by thiol‑ene reaction. European Polymer Journal, 2015, 67: 439‑448.
- [2]. Jatin J. Lade, et al. The remarkable journey of catalysts from stoichiometric to catalytic quantity for allyltrimethylsilane inspired allylation of acetals, ketals, aldehydes and ketones. RSC Adv. 2017; 7 (13): 8011-8033.
- [3]. Sommer L H, et al. Reactions of Allyltrimethylsilane. Journal of the American Chemical Society, 1948, 70(9): 2872‑2874.
Keywords
