38274-75-8 Usage
Chemical Structure
A naphthyl group attached to a silicon atom.
Specific Content
The naphthyl group consists of a fused benzene ring system, while the silicon atom provides a stable and reactive center for bond formation.
Specific Content
1-Naphthylsilicon can be used in a wide range of chemical reactions, such as the formation of carbon-silicon bonds, which are essential in creating complex organic molecules.
Specific Content
The silicon atom in 1-naphthylsilicon can easily form bonds with carbon atoms, leading to the creation of new compounds and materials.
Specific Content
1-Naphthylsilicon contributes to the development of advanced materials, such as silicon polymers with unique properties and a variety of organosilicon compounds for various applications.
Specific Content
The combination of the naphthyl group and the silicon atom in 1-naphthylsilicon provides a distinct structure that enables it to engage in numerous chemical reactions, making it a valuable building block in organic synthesis.
Specific Content
1-Naphthylsilicon can be utilized in the creation of innovative materials, such as optoelectronic devices and sensors, which have potential applications in various industries and technologies.
Specific Content
As a key building block in organic synthesis and material science, 1-naphthylsilicon offers diverse opportunities for the development of novel compounds, materials, and technologies.
Versatility in Organic Synthesis
A valuable reagent for various transformations.
Formation of Carbon-Silicon Bonds
Efficient reagent for bond formation.
Production of Silicon-Based Materials
Used in the synthesis of silicon polymers and organosilicon compounds.
Unique Structure
Allows participation in a wide range of chemical reactions.
Potential Applications
Development of new materials with unique properties.
Role in Organic Synthesis and Material Science
A crucial compound for innovation and technological advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 38274-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,7 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38274-75:
(7*3)+(6*8)+(5*2)+(4*7)+(3*4)+(2*7)+(1*5)=138
138 % 10 = 8
So 38274-75-8 is a valid CAS Registry Number.
38274-75-8Relevant articles and documents
Electrochemical properties of arylsilanes
Biedermann, Judith,Wilkening, H. Martin R.,Uhlig, Frank,Hanzu, Ilie
, p. 13 - 18 (2019/03/27)
In the past, the electrochemical properties of organosilicon compounds were investigated for both fundamental reasons and synthesis purposes. Little is, however, known about the electrochemical behaviour of hydrogen-bearing arylsilanes. Here, we throw light on the electrochemical properties of 11 arylsilanes compounds, 2 of them synthesized for the first time. The oxidation potentials are found to depend on both the nature and number of the aryl groups. Based on these findings it was possible to establish some variation trends that match the expected structure–property correlations. Furthermore, we present first insights into the electrochemical reaction kinetics behind and identify several soluble electrochemical oxidation products.
Carbon-Silicon Bond Formation in the Synthesis of Benzylic Silanes
Visco, Michael D.,Wieting, Joshua M.,Mattson, Anita E.
, p. 2883 - 2885 (2016/07/06)
Sterically encumbered organosilanes can be difficult to synthesize with conventional, strongly basic reagents; the harsh reaction conditions are often low yielding and not suitable for many functional groups. As an alternative to the typical anionic strat
Pentacoordinate silicon compounds. Reactions of silatranes with nucleophiles
Cerveau, G.,Chuit, C.,Corriu, R. J. P.,Nayyar, N. K.,Reye, C.
, p. 159 - 168 (2007/10/02)
The reactions of hydro, organyl and halosilatranes with nucleophiles have been studied.Substitution involving cleavage of equatorial Si-O bonds is always observed.Silitranes exhibit reactivity quite different from that of analogous trialkoxysilanes or anionic pentacoordinate silicon compounds.
