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Cyclohexyl(methyl)silane is an organosilicon compound with the chemical formula C7H16Si. It is a colorless liquid at room temperature and is derived from the combination of cyclohexane and methyl groups with a silicon atom. cyclohexyl(methyl)silane is widely used in various applications, including as a coupling agent in the production of composite materials, as a release agent in the rubber and plastics industry, and as a precursor in the synthesis of other organosilicon compounds. Cyclohexyl(methyl)silane is known for its stability, low toxicity, and ability to form strong bonds with inorganic materials, making it a valuable component in the development of new materials and technologies.

2096-99-3

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2096-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2096-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2096-99:
(6*2)+(5*0)+(4*9)+(3*6)+(2*9)+(1*9)=93
93 % 10 = 3
So 2096-99-3 is a valid CAS Registry Number.

2096-99-3Downstream Products

2096-99-3Relevant academic research and scientific papers

POLYMERIZABLE MONOMER SUITABLE FOR DENTAL MATERIAL, AND DENTAL COMPOSITION BASED ON THE SAME

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Paragraph 0123; 0126, (2019/07/25)

PROBLEM TO BE SOLVED: To provide a polymerizable monomer useful for a dental composite resin which has small polymerization shrinkage in curing, excellent operability, excellent mechanical strength of cured products, and a thermal expansion coefficient co

Synthesis of hydrosilanes: Via Lewis-base-catalysed reduction of alkoxy silanes with NaBH4

Aoyagi, Keiya,Ohmori, Yu,Inomata, Koya,Matsumoto, Kazuhiro,Shimada, Shigeru,Sato, Kazuhiko,Nakajima, Yumiko

supporting information, p. 5859 - 5862 (2019/05/27)

Hydrosilanes were synthesized by reduction of alkoxy silanes with BH3 in the presence of hexamethylphosphoric triamide (HMPA) as a Lewis-base catalyst. The reaction was also achieved using an inexpensive and easily handled hydride source NaBH4, which reacted with EtBr as a sacrificial reagent to form BH3in situ.

Catalytic oxidation of diorganosilanes to 1,1,3,3-tetraorganodisiloxanes with gold nanoparticle assembly at the water-chloroform interface

Shankar, Ravi,Sharma, Asmita,Jangir, Bhawana,Chaudhary, Manchal,Kociok-K?hn, Gabriele

, p. 813 - 819 (2019/01/09)

The formation of the spherical self-assembly of gold nanoparticles (AuNPs) of 200 ± 20 nm size at the water-chloroform interface is achieved by employing the cyclotetrasiloxane [RSCH2CH2SiMeO]4 (R = CH2CH2OH) as the stabilizing ligand. The interfacially stabilized AuNPs act as a versatile catalyst for selective hydrolytic oxidation of only one of the Si-H bonds in secondary organosilanes, RR1SiH2 (R, R1 = alkyl, aryl, and sila-alkyl), to afford the high yield synthesis of 1,1,3,3-tetraorganodisiloxanes, (HRR1Si)2O. The study unravels for the first time the role of the photothermal effect arising from the excitation of the surface plasmon resonance of the AuNPs under visible light irradiation in enhancing the catalytic activity at ambient temperature.

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