63103-39-9 Usage
Uses
Used in Organic Synthesis:
Phosphine oxide, diphenyl[2-(trimethylsilyl)ethyl]is utilized as a catalyst or reagent in organic synthesis reactions due to its ability to facilitate and enhance the efficiency of various chemical transformations. Its unique structure allows it to participate in a wide range of reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Organometallic Chemistry:
In the field of organometallic chemistry, Phosphine oxide, diphenyl[2-(trimethylsilyl)ethyl]serves as a ligand, forming coordination complexes with transition metals. This role is crucial for the stabilization and reactivity of organometallic compounds, which are essential in various catalytic processes and homogeneous catalysis.
Used in Materials Science:
Phosphine oxide, diphenyl[2-(trimethylsilyl)ethyl]may have potential applications in materials science, where its unique properties could contribute to the development of new materials with specific characteristics. Its ability to form stable complexes with metals could be particularly useful in creating materials with tailored properties for various applications.
Used as a Building Block in Synthesis:
This phosphine oxide derivative also serves as a building block for the synthesis of more complex organic compounds. Its structural features make it a suitable precursor for the construction of larger molecules with diverse functionalities, which can be applied across various industries and research areas.
Check Digit Verification of cas no
The CAS Registry Mumber 63103-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63103-39:
(7*6)+(6*3)+(5*1)+(4*0)+(3*3)+(2*3)+(1*9)=89
89 % 10 = 9
So 63103-39-9 is a valid CAS Registry Number.
63103-39-9Relevant academic research and scientific papers
The lithiation reactivity and selectivity of differentially branched alkyldiphenylphosphine oxides - A simple and versatile approach to ortho-functionalized arylphosphine oxides
Mahamulkar, Shraddha G.,Císa?ová, Ivana,Jahn, Ullrich
supporting information, p. 793 - 799 (2015/03/18)
Alkyldiphenylphosphine oxides typically undergo α-deprotonation with alkyllithium reagents. Here, the lithiation of differentially branched alkyldiphenylphosphine oxides was investigated and a diverse, but predictable reactivity was found. γ-Branched deri
Photoinduced hydrophosphinylation of alkenes with diphenylphosphine oxide
Kawaguchi, Shin-ichi,Nomoto, Akihiro,Sonoda, Motohiro,Ogawa, Akiya
scheme or table, p. 624 - 626 (2011/02/28)
Photoinduced hydrophosphinylation of alkenes with diphenylphosphine oxide took place regioselectively affording the corresponding phosphine oxide in good yields. This hydrophosphinylation is of simple operation and widely tolerant to a variety of the functionalities.
