70531-02-1 Usage
Description
1-PHENYL-2-TRIMETHOXY SILYL ETHENE is a chemical compound that is commonly used as a reagent in organic synthesis. It is a derivative of ethene with a phenyl group and three trimethoxy silyl groups attached to the carbon atoms. 1-PHENYL-2-TRIMETHOXY SILYL ETHENE is known for its ability to undergo various reactions, including cross-coupling reactions and polymerization, making it a versatile compound with a wide range of applications in organic chemistry.
Uses
Used in Organic Synthesis:
1-PHENYL-2-TRIMETHOXY SILYL ETHENE is used as a reagent for the preparation of various organic compounds and materials. Its unique structure allows it to participate in a variety of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Cross-Coupling Reactions:
In cross-coupling reactions, 1-PHENYL-2-TRIMETHOXY SILYL ETHENE serves as a key intermediate, facilitating the formation of new carbon-carbon bonds. This property is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Polymerization:
1-PHENYL-2-TRIMETHOXY SILYL ETHENE is also utilized in polymerization processes, where it contributes to the formation of polymers with specific properties. These polymers can be used in various industries, such as plastics, coatings, and adhesives.
Used in the Production of Functionalized Materials:
1-PHENYL-2-TRIMETHOXY SILYL ETHENE is employed in the synthesis of functionalized materials, which possess tailored properties for specific applications. These materials can be used in high-tech industries, such as electronics, where they can serve as components in devices or contribute to improved performance.
Used in the Development of Novel Chemical Processes:
1-PHENYL-2-TRIMETHOXY SILYL ETHENE plays a role in the research and development of new chemical processes, where it can be used to explore innovative synthetic routes and improve existing ones. This contributes to the advancement of organic chemistry and the discovery of new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 70531-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,3 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70531-02:
(7*7)+(6*0)+(5*5)+(4*3)+(3*1)+(2*0)+(1*2)=91
91 % 10 = 1
So 70531-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3Si/c1-12-15(13-2,14-3)10-9-11-7-5-4-6-8-11/h4-10H,1-3H3/b10-9+
70531-02-1Relevant articles and documents
Heterogeneous hydrosilylation reaction catalysed by platinum complexes immobilized on bipyridine-periodic mesoporous organosilicas
Naganawa, Yuki,Maegawa, Yoshifumi,Guo, Haiqing,Gholap, Sandeep Suryabhan,Tanaka, Shinji,Sato, Kazuhiko,Inagaki, Shinji,Nakajima, Yumiko
, p. 5534 - 5540 (2019/05/10)
The utility of a bipyridine periodic mesoporous organosilica, BPy-PMO, as a support material of a hydrosilylation catalyst was investigated in the hydrosilylation of phenylacetylene with trimethoxysilane. [PtMe2(BPy-PMO)] (1) exhibited a modera
N-heterocyclic carbene platinum complexes functionalized with a polyether chain and silyl group: Synthesis and application as a catalyst for hydrosilylation
Zhang, Fengxiang,Bai, Ying,Yang, Xiaoling,Li, Jiayun,Peng, Jianjian
, p. 1271 - 1278 (2017/10/18)
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Hydrosilylation of alkynes catalysed by platinum on titania
Alonso, Francisco,Buitrago, Robison,Moglie, Yanina,Ruiz-Martínez, Javier,Sepúlveda-Escribano, Antonio,Yus, Miguel
experimental part, p. 368 - 372 (2011/02/16)
The heterogeneous hydrosilylation of alkynes catalysed by platinum on titania is reported. A variety of hydrosilanes react with both terminal and internal alkynes to furnish the corresponding vinyl silanes in high yields and short reaction times as well as in a regio- and stereoselective manner. The catalyst can be easily recovered and reused in several consecutive cycles.
