80399-29-7

Usage

Uses

Used in Silicone Polymer and Resin Production:
Trimethylsiloxyvinyldimethyl carbinol is used as a coupling agent in the production of silicone polymers and resins. Its reactive vinyl group enables it to effectively bond with other components, enhancing the overall properties and performance of the resulting materials.
Used in Coatings and Adhesives Industry:
In the coatings and adhesives industry, trimethylsiloxyvinyldimethyl carbinol is utilized as a surface modifier. Its ability to participate in crosslinking reactions contributes to the improvement of adhesion, durability, and overall performance of the coatings and adhesives.
Used in Specialty Chemical Product Manufacturing:
Trimethylsiloxyvinyldimethyl carbinol is a key ingredient in the production of specialty chemical products such as siloxane resins and silane coupling agents. Its presence in these products is crucial for achieving desired properties and performance characteristics in various applications.

InChI:InChI=1/C8H18O2Si/c1-8(2,9)6-7-10-11(3,4)5/h6-7,9H,1-5H3/b7-6+

Upstream product

• 78-85-3 2-methylpropenal 
• 13170-43-9 (trimethylsilyl)methylmagnesium chloride 
• 18293-99-7 Prenyltrimethylsilane 
• 503-60-6 3,3-dimethyl-allyl chloride 

Downstream Products

• 4111-01-7 4-methyl-4-vinylcyclohexan-1-one 
• 116078-54-7 4(S)-benzyl-N-<4'-methyl-6'-(trimethylsilyl)-4'-hexenoyl>oxazolidinone 
• 116078-55-8 (2'S,4S)-4-benzyl-N-<2',4'-dimethyl-6'-(trimethylsilyl)-4'-hexenoyl>oxazolidinone 

Relevant academic research and scientific papers

Efficient construction of the clerodane decalin core by an asymmetric Morita-Baylis-Hillman reaction/Lewis acid promoted annulation strategy

(Chemical Equation Presented) Linking rings: A general route toward the clerodane diterpene core using an asymmetric Morita-Baylis-Hillman (MBH)/ Lewis acid mediated ring-annulation process has been developed. The scope of the asymmetric Bronsted acid cat

A regiodefined synthesis of α-trimethylsilyl ketones catalyzed by rhodium(I) hydride complex

Regiodefined synthesis of α-trimethylsilyl ketones is attained by one of three different routes: isomerization of β-trimethylsilyl allyl alcohols (route A), isomerization of β'-trimethylsilyl allyl alcohols (route B), and dehydrogenation of β-trimethylsil

ENE-REACTIVITE D'ALLYLSILANES: FONCTIONNALISATION ET REGIOCHIMIE

The hydroperoxidation of various allylsilanes by singlet oxygen has been studied.The regioselectivity of this reaction compared to those of ethyl azodicarboxylate and 4-phenyl-1,2,4-triazoline-3,5-dione, is discussed.Mechanisms are considered in the general field of the ene reaction applied to allylic organometallic Group IVB compounds.The structures of the new products (alcohols, urazoles, hydrazines) have been determined, directly or after transformations, by NMR spectroscopy.