55811-60-4 Usage
Uses
Used in Organic Synthesis:
5-METHYL-2-TRIMETHYLSILYL-FURAN is used as a building block for [creating new chemical structures] because of its reactivity with other compounds, allowing for the development of novel organic molecules.
Used in Research Applications:
In the field of research, 5-METHYL-2-TRIMETHYLSILYL-FURAN is used as a [reagent] for [exploring its aromatic properties and reactivity in various chemical reactions], contributing to the advancement of chemical knowledge and the discovery of new compounds.
Used in Industrial Applications:
5-METHYL-2-TRIMETHYLSILYL-FURAN is used as a [chemical intermediate] in industrial processes for [producing a variety of end products], leveraging its ability to form new chemical structures that may have specific applications in different industries.
Used in Controlled Laboratory Environments:
Due to its potentially hazardous nature, 5-METHYL-2-TRIMETHYLSILYL-FURAN is used in [laboratory settings] for [careful handling and experimentation] to ensure safety and proper utilization of its chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 55811-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,1 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55811-60:
(7*5)+(6*5)+(5*8)+(4*1)+(3*1)+(2*6)+(1*0)=124
124 % 10 = 4
So 55811-60-4 is a valid CAS Registry Number.
55811-60-4Relevant academic research and scientific papers
Cleavage of Furan-2-yl, 2-Thienyl-, Benzofuran-2-yl-, and Benzothiophen-2-yl-methyl(trimethyl)silanes (RCH2SiMe3) by Methanolic Sodium Methoxide; Acidities of the Corresponding RCH3 Species
Dembech, Pasquale,Seconi, Giancarlo,Eaborn, Colin,Rodriguez, Juan A.,Stamper, John G.
, p. 197 - 198 (2007/10/02)
Rates of cleavage of RCH2SiMe3 by 2.00M-NaOMe in MeOH or MeOD at 50 deg C have been determined for R = furan-2-yl, 2-thienyl, benzofuran-2-yl, and benzothiophen-2-yl; the values of 1E5ks in MeOH and (in parentheses) in MeOD, where ks is the specific second order rate constant, are, respectively: 0.070 (0.167), 0.26 (0.52), 165 (310), and 70 (130) dm3 mol-1 s-1.The values of the ratios of ks in MeOH to hat in MeOD are in the range 0.42-0.54, consistent with rate-determining separation of the carbanion RCH2-. s is 1.57 (1.55), the ratio is 1.01, consistent with electrophilic assistance by proton transfer from the solvent to the separating carbon centre.> The results are discussed in the light of the deprotonation energies calculated (STO-3G) for the corresponding carbon acids RCH3, and approximate pKa values are derived for the latter, viz. (R =) furan-2-yl, 40.6; 2-thienyl, 39.7; benzofuran-2-yl, 35.2; benzothiophen-2-yl, 35.8.
