2917-63-7 Usage
Uses
Used in Organic Synthesis:
[dimethyl(propyl)silyl]methyl acetate is utilized as a silylating agent, playing a crucial role in protecting alcohols and phenols from experiencing unwanted side reactions during the synthesis process. Its ability to shield these functional groups allows for cleaner reactions and improved yields of desired products.
Used in Analytical Chemistry:
In the field of analytical chemistry, [dimethyl(propyl)silyl]methyl acetate serves as a reagent for the derivatization of analytes. This process is essential for gas chromatography-mass spectrometry (GC-MS) analysis, where it enhances the volatility and stability of certain compounds, facilitating their detection and analysis.
Used in the Production of Siloxane-based Materials and Polymers:
[dimethyl(propyl)silyl]methyl acetate's silyl functionality makes it a valuable component in the creation of various siloxane-based materials and polymers. These materials are known for their unique properties, such as thermal stability, low surface tension, and resistance to extreme temperatures, making them suitable for a wide range of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2917-63-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2917-63:
(6*2)+(5*9)+(4*1)+(3*7)+(2*6)+(1*3)=97
97 % 10 = 7
So 2917-63-7 is a valid CAS Registry Number.
2917-63-7Relevant academic research and scientific papers
Synthesis and thermal stability of silicon-containing esters of phosphorus acids 5.* the relative migration ability of substituents at the silicon atom in the thermal rearrangement of trialkylsilylmethyl diphenyl phosphates
Zakharov,Molchanova,Shcherbina,Petrovskii,Kabachnik
, p. 1718 - 1724 (2007/10/03)
A number of trialkylsilylmethyl diphenyl phosphates MeRR'SiCH2OP(O)(OPh)2 (Ia-e: R = Et (a), Pr (b), CF3CH2CH2 (c, e), Me3SiCH2 (d); R' = Me (a-d), Et (e)) were synthesized and their thermal rearrangement, of the 1,2-shift type, was studied. The rearrangement consists of the migration of an alkyl group from Si atom to the methylene carbon atom and gives the corresponding silyl esters. The rate of the rearrangement was found to increase in the order 1d 3CH2CH2 3SiCH2, which differs substantially from the order in which the rate of the rearrangement of phosphates 1a-d changes. The electro-negativity of the migrating group affects noticeably the relative ability to migrate.
