1825-71-4

Usage

Uses

Used in Adhesives and Sealants Industry:
Chlorodimethylisopropoxysilane is used as a coupling agent and surface modifier for enhancing the bonding properties and durability of adhesives and sealants. Its reactivity and ability to undergo hydrolysis make it an effective crosslinking agent, improving the performance and longevity of these products.
Used in Coatings Industry:
In the coatings industry, CDIS is used as a coupling agent to improve the adhesion and durability of coatings on various substrates. Its reactive nature allows it to form strong bonds with the substrate, resulting in coatings with enhanced performance and resistance to wear and environmental factors.
Used in Silicone Polymers and Resins Synthesis:
Chlorodimethylisopropoxysilane is used as a crosslinking agent in the synthesis of silicone polymers and resins. Its ability to undergo hydrolysis in the presence of moisture enables the formation of stable crosslinks, which contribute to the overall strength and stability of the resulting polymers and resins.
Used in Silicone Rubbers Manufacturing:
CDIS is a key ingredient in the manufacturing of silicone rubbers, where it functions as a coupling agent and surface modifier. Its reactivity and hydrolysis properties contribute to the improved bonding properties and durability of silicone rubbers, making them suitable for various applications, including automotive and construction industries.
Used as a Water Repellent and Surface Treatment Agent:
In the construction and automotive industries, chlorodimethylisopropoxysilane is used as a water repellent and surface treatment agent. Its ability to form stable bonds with various substrates makes it an effective agent for improving the water resistance and surface properties of materials, enhancing their performance and longevity.

Upstream product

• 75-78-5 dimethylsilicon dichloride 
• 67-63-0 isopropyl alcohol 
• 17877-29-1 butoxy-isopropoxy-dimethyl-silane 
• 1719-53-5 diethyldichlorosilane 

Downstream Products

• 140438-41-1 C₂₁H₃₃NOSi₂ 
• 126918-18-1 (2S,3R)-2-(2,4-difluorophenyl)-1-(dimethylisopropoxysilyl)-3-(2-tetrahydropyranyloxy)-2-butanol 
• 126918-18-1 (2R,3S)-2-(2,4-Difluoro-phenyl)-1-(isopropoxy-dimethyl-silanyl)-3-(tetrahydro-pyran-2-yloxy)-butan-2-ol 
• 17988-21-5 dimethyl(isopropoxy)phenylsilane 

Relevant academic research and scientific papers

A heteroatom-containing aromatic vinyl compound (by machine translation)

[Problem] heteroatom containing aromatic vinyl compound at high purity, high yield manufacturing method capable of manufacturing. (I) formula [a]: R1 - R2 - Y (where, R1 A specific aromatic group, R2 The Si (Rs

Cobalt-Mediated [2+2+2] Cycloadditions of Alkynes to Benzo-[ b ]furans and Benzo[ b ]thiophenes: A Potential Route toward Morphanoids

Exploratory studies of the CpCo-mediated [2+2+2] cycloaddition of alkynes to the 2,3-double bond of benzo[ b ]furans (and some benzo[ b ]thiophenes) are presented, with the general aim to access morphinan substructures. The basic feasibility of constructing Co-complexed tetrahydrophenanthro[4,5- bcd ]furans (and -thiophenes) in moderate to good yields is demonstrated, with complete to extensive diastereoselectivity. Limitations are the apparent necessity for bulky (silylated) monoalkynes, the lack of regioselectivity in the cocyclization with unsymmetrical alkynes, and the sensitivity of the ligands, both complexed and uncomplexed, with respect to ring opening and rearrangement.

1,3 DIHYDROFURO [3,4-c]PYRIDINES AND THEIR PREPARATION

The present invention relates to novel 1,3-dihydrofuro[3,4-c]pyridines which are useful intermediates in the synthesis of pyridoxines and a method for their preparation by cobalt(I) complex-catalysed [2 + 2 + 2]-cycloaddition of di-[(3-dimethyl-C1-4-alkoxysilyl)-2-propynyl)] ethers with acetonitrile.

Regioselective alkylation of 1-silyl-2-methylallyl carbanions

Regioselective alkylations of 1-silyl-2-methylallyl carbanions were achieved by changing the substituents on silicon. γ-Alkylation was favoured by dialkylamino group on silicon, whereas α-alkylation was favoured by an alkoxy substituent on silicon.