62761-90-4 Usage
Uses
Used in Organic Synthesis:
Silane, [(phenylthio)methylene]bis[trimethylis used as a versatile intermediate in organic synthesis for the preparation of various organic compounds. Its unique structure allows for selective reactions and transformations, making it a valuable building block in the synthesis of complex organic molecules.
Used in Vinylsilane Formation:
Phenylthiobis(trimethylsilyl)methane is used as a precursor in the formation of vinylsilanes. Vinylsilanes are important intermediates in the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and materials. The ability to generate vinylsilanes from this silane compound provides a convenient and efficient route to these valuable intermediates.
Used as a Methoxycarbonyl Anion Equivalent:
In addition to its use in vinylsilane formation, Silane, [(phenylthio)methylene]bis[trimethylalso serves as a methoxycarbonyl anion equivalent. This property allows it to be used in various organic reactions, such as the synthesis of esters, carbonates, and other carboxylic acid derivatives. Its reactivity as a methoxycarbonyl anion equivalent makes it a useful tool in the development of new synthetic methods and the preparation of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 62761-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,6 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62761-90:
(7*6)+(6*2)+(5*7)+(4*6)+(3*1)+(2*9)+(1*0)=134
134 % 10 = 4
So 62761-90-4 is a valid CAS Registry Number.
62761-90-4Relevant academic research and scientific papers
REACTIONS OF PHENYLTHIOTRIMETHYISILYLMETHYLLITHIUM: PREPARATION OF α-PHENYLTHIOKETONES AND ADDITIONS TO 2-CYCLOHEXEN-1-ONE
Ager, David J.
, p. 2803 - 2806 (2007/10/02)
Phenylthiotrimethylsilylmethyllithium(1) was reacted with a variety of electrophiles, including some containing two functional groups. α-Phenylthioketones were obtained from the reaction with esters.The anion(1) underwent either 1,2- or 1,4-addition, depe
