2917-56-8 Usage
Uses
Used in Organic Synthesis:
[ethyl(dimethyl)silyl]methanol is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions and improve overall yields. Its organosilicon nature allows for unique interactions and transformations that are not possible with other types of reagents.
Used in Protective Groups for Alcohols:
In organic chemistry, [ethyl(dimethyl)silyl]methanol serves as a protective group for alcohols. This application is crucial for preventing unwanted side reactions and ensuring the selective functionalization of other groups in a molecule.
Used in Pharmaceutical Synthesis:
[ethyl(dimethyl)silyl]methanol is used as a building block in the synthesis of pharmaceuticals. Its unique properties and reactivity enable the creation of complex molecular structures that are essential for the development of new drugs.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, [ethyl(dimethyl)silyl]methanol is employed as a building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its contribution to the development of these products is vital for enhancing agricultural productivity and crop protection.
Safety Precautions:
Given its flammable nature and potential hazards if inhaled, swallowed, or absorbed through the skin, [ethyl(dimethyl)silyl]methanol requires proper safety precautions during handling and storage. It is essential to follow established safety guidelines and protocols to minimize risks and ensure the safe use of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 2917-56-8 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, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2917-56:
(6*2)+(5*9)+(4*1)+(3*7)+(2*5)+(1*6)=98
98 % 10 = 8
So 2917-56-8 is a valid CAS Registry Number.
2917-56-8Relevant 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.
