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Usage

Uses

Used in Silicone Polymer Production:
CHLOROMETHYLTRIISOPROPOXYSILANE 96 is used as a crosslinking agent in the production of silicone rubber, contributing to the formation of a stable and elastic polymer network.
Used in Adhesives, Sealants, and Coatings:
In the formulation of adhesives, sealants, and coatings, CHLOROMETHYLTRIISOPROPOXYSILANE 96 serves as a coupling agent, enhancing the bonding strength and durability of these materials.
Used in Electronics Industry:
CHLOROMETHYLTRIISOPROPOXYSILANE 96 is utilized in the manufacturing of electronic components, where its properties contribute to the creation of reliable and high-performance devices.
Used in Surface Modification:
For surface modification applications, CHLOROMETHYLTRIISOPROPOXYSILANE 96 is used to improve adhesion and moisture resistance, making it suitable for various substrates in different industries.
Safety Precautions:
Due to its hazardous nature, CHLOROMETHYLTRIISOPROPOXYSILANE 96 should be handled with caution to avoid skin, eye, and respiratory system irritation upon contact or inhalation.

InChI:InChI=1/C10H23ClO3Si/c1-8(2)12-15(7-11,13-9(3)4)14-10(5)6/h8-10H,7H2,1-6H3

Upstream product

• 1558-25-4 (chloromethyl)trichlorosilane 
• 67-63-0 isopropyl alcohol 

Relevant academic research and scientific papers

Synthesis of 2,2,5,5-Tetrasubstituted 1,4-Dioxa-2,5-disilacyclohexanes via Organotin(IV)-Catalyzed Transesterification of (Acetoxymethyl)alkoxysilanes

(Acetoxymethyl)silanes 2, 7 a-c, and 10 a-c with at least one alkoxy group, of the general formula (AcOCH2)Si(OR)3-n(CH 3)n (R: Me, Et, iPr; n=0, 1, 2), were synthesized from the corresponding (chloromethyl)silanes 1, 6 a-c, and 9 a-c by treatment with potassium acetate under phase-transfer-catalysis conditions. These compounds were found to provide 2,2,5,5-organo-substituted 1,4-dioxa-2,5- disilacyclohexanes 3, 8 a-c, and 11 a-c if treated with organotin(IV) catalysts such as dioctyltin oxide. The reaction proceeds through transesterification of the acetoxy and alkoxy units followed by ring-closure to form a dimeric six-membered ring. The corresponding alkyl acetates are formed as the reaction by-products. With these mild conditions, the method overcomes the drawbacks of previously reported synthetic routes to furnish 2,2,5,5-tetramethyl-1,4-dioxa-2, 5-disilacyclohexane (3) and even allows the synthesis of 1,4-dioxa-2,5- disilacyclohexanes bearing hydrolytically labile alkoxy substituents at the silicon atom in good yields and high purity. These new materials were fully characterized by NMR spectroscopy, elemental analysis, mass spectrometry, and X-ray analysis (trans-8 a). Tin makes the ring! Easily accessible (acetoxymethyl)silanes with at least one alkoxy group give 2,2,5,5-organo- substituted 1,4-dioxa-2,5-disilacyclohexanes (see figure) in good yields and high purity when treated with organotin(IV) catalysts. The mild reaction conditions even allowed the synthesis of cyclic silanes with hydrolytically labile alkoxy substituents. Copyright

LOW MOLECULAR WEIGHT CARBOSILANES, PRECURSORS THEREOF, AND METHODS OF PREPARATION

A series of silicon compounds are provided, which are excellent precursors to small carbosilanes, such as 1,3,5-trisilapentane, 2,4,6-trisilaheptane, tris(silylmethyl)silane and tetrakis(silylmethyl)silane. A method of preparing a carbosilane involves forming a Grignard, lithium, or metallic reagent from a halomethyltrialkoxysilane, reacting the Grignard, lithium, or metallic reagent with a dihalodihydridosilane, a trihalohydridosilane, a tetrahalosilane, a dialkoxydihydridosilane, a trialkoxyhydridosilane, or a tetraalkoxysilane to yield a carbosilane precursor, and reducing the precursor to form the carbosilane.