756-81-0 Usage
Uses
Used in Chemical Synthesis:
Dimethyldiethylsilane is used as a reagent for the synthesis of various organic compounds, contributing to the creation of a wide array of products across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Dimethyldiethylsilane is utilized for the synthesis of pharmaceutical compounds, leveraging its reducing properties and its ability to act as a source of silanolate nucleophiles to facilitate the production of medicinal agents.
Used in Silicone Polymer Production:
Dimethyldiethylsilane is employed as a key component in the production of silicone polymers, which are used in a variety of applications, including sealants, adhesives, and medical devices, due to their unique properties such as heat resistance and flexibility.
Used in Material Science:
In the field of material science, Dimethyldiethylsilane is used to develop new materials with specific properties, such as thermal stability and chemical resistance, by participating in the synthesis of advanced composites and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 756-81-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 756-81:
(5*7)+(4*5)+(3*6)+(2*8)+(1*1)=90
90 % 10 = 0
So 756-81-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H16Si/c1-5-7(3,4)6-2/h5-6H2,1-4H3
756-81-0Relevant academic research and scientific papers
Wagner-Meerwein-Type Rearrangements of Germapolysilanes - A Stable Ion Study
Albers, Lena,Meshgi, Mohammad Aghazadeh,Baumgartner, Judith,Marschner, Christoph,Müller, Thomas
supporting information, p. 3756 - 3763 (2015/08/19)
(Chemical Equation Presented). The rearrangement of tris(trimethylsilyl)silyltrimethylgermane 1 to give tetrakis(trimethylsilyl)germane 2 was investigated as a typical example for Lewis acid catalyzed Wagner-Meerwein-type rearrangements of polysilanes and polygermasilanes. Direct 29Si NMR spectroscopic evidence is provided for several cationic intermediates during the reaction. The identity of these species was verified by independent synthesis and NMR characterization, and their transformation was followed by NMR spectroscopy.
