51075-23-1 Usage
Uses
Used in Organic Synthesis:
Trimethyl[(2-phenylprop-1-yl)oxy]silane serves as a coupling agent in organic synthesis reactions, particularly for the formation of silicone polymers. Its ability to increase reactivity and compatibility with various organic compounds makes it an indispensable tool in the synthesis of complex organic molecules.
Used in Adhesion and Bonding Applications:
In various industries, trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is utilized to improve the adhesion and bonding properties of materials. Its capacity to enhance the interfacial interactions between different materials contributes to the development of stronger and more durable products.
Used in Polymer Industry:
Trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is used as a coupling agent in the polymer industry for the synthesis of silicone polymers. Its role in facilitating the formation of these polymers is crucial for creating materials with specific properties tailored to various applications.
Used in Chemical Additive Industry:
As a valuable additive, trimethyl[(2-phenylprop-1-en-1-yl)oxy]silane is incorporated into formulations to enhance the performance of products in the chemical industry. Its contribution to improving adhesion and bonding makes it a sought-after component in the development of high-quality industrial and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 51075-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51075-23:
(7*5)+(6*1)+(5*0)+(4*7)+(3*5)+(2*2)+(1*3)=91
91 % 10 = 1
So 51075-23-1 is a valid CAS Registry Number.
51075-23-1Relevant academic research and scientific papers
Preparation of silyl enol ethers using (bistrimethylsilyl)acetamide in ionic liquids
Smietana, Michael,Mioskowski, Charles
, p. 1037 - 1039 (2007/10/03)
(matrix presented) Ionic liquids have been used for the preparation of silyl enol ethers from aldehydes and ketones with (bistrimethylsilyl)acetamide (BSA) in good yields.
High Pressure Reaction of 1-Methoxy-3-trialkylsiloxybuta-1,3-diene with Aldehydes. Cycloaddition or Silicon Migration Reaction
Yamamoto, Yoshinori
, p. 945 - 946 (2007/10/02)
The high pressure reaction of Danishefsky's diene with aromatic aldehydes produces the cycloadduct, while with an aliphatic aldehyde such as 2-phenylpropionaldehyde the intermolecular silicon migration from oxygen to oxygen takes place.
UNERWARTETE REAKTIONSPRODUKTE VON N-METHYL-N-TRIMETHYLSILYLTRIFLUORACETAMID (MSTFA) MIT ALDEHYDEN
Ende, M.,Luftmann, H.
, p. 5167 - 5170 (2007/10/02)
Aldehydes react with MSTFA (N-methyl-N-trimethylsilyl-trifluoroacetamide) to give E/Z-silylenolethers and surprisingly addition products of the reagent to the carbonyl group.The mass spectra of the MSTFA/aliphatic aldehyde adducts are dominated by a key fragment of m/z 228 formed by elimination of the alkyl part.With MSTFA/aromatic aldehyde adducts this fragmentation is replaced by M-H and M-CH3N.8COCF3 (M-126 amu) ions.
