853955-71-2 Usage
Uses
Used in Organic Synthesis:
2-[Dimethyl(2-methylphenyl)silyl]phenylmethanol is used as a reagent in organic synthesis for [application reason]. Its unique properties allow it to facilitate various chemical reactions and contribute to the formation of complex organic molecules.
Used in Protective Group Chemistry:
In the field of chemistry, 2-[Dimethyl(2-methylphenyl)silyl]phenylmethanol is used as a protective group in chemical reactions for [application reason]. Its ability to shield reactive sites during synthesis helps prevent unwanted side reactions and ensures the desired product formation.
Used in Pharmaceutical Industry:
2-[Dimethyl(2-methylphenyl)silyl]phenylmethanol is also utilized in the pharmaceutical industry for [application reason]. Its role in the synthesis of complex drug molecules and its protective group function can be crucial in the development of new pharmaceuticals.
Used in Chemical Research:
In the realm of chemical research, 2-[Dimethyl(2-methylphenyl)silyl]phenylmethanol is employed for [application reason]. Its unique properties and reactivity make it a valuable tool for exploring new chemical pathways and understanding the underlying mechanisms of various reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 853955-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,9,5 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 853955-71:
(8*8)+(7*5)+(6*3)+(5*9)+(4*5)+(3*5)+(2*7)+(1*1)=212
212 % 10 = 2
So 853955-71-2 is a valid CAS Registry Number.
853955-71-2Relevant academic research and scientific papers
Silicon-Based Cross-Coupling Reagent and Production Method of Organic Compound Using the Same
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Page/Page column 15, (2009/04/24)
In one embodiment of the present invention, a silicon-based cross-coupling reagent is disclosed which is a highly stable tetraorganosilicon compound allowing for a cross-coupling reaction under mild reaction conditions without using fluoride ions, transition metal promoter, or strong bases, and the residue of the silicon reagent can be recovered and reused. The silicon-based cross-coupling reagent is a silicon compound in which an o-hydroxymethylphenyl group is connected to a silicon atom for intramolecular activation.
Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes: An entry to tetraorganosilicon reagents for the silicon-based cross-coupling reaction
Nakao, Yoshiaki,Imanaka, Hidekazu,Sahoo, Akhila K.,Yada, Akira,Hiyama, Tamejiro
, p. 6952 - 6953 (2007/10/03)
Alkenyl- and aryl[2-(hydroxymethyl)phenyl]dimethylsilanes, highly stable tetraorganosilicon reagents, are found to react with aryl and alkenyl iodides in the presence of a palladium catalyst and K2CO3 as a base, significantly milder conditions compared with those ever reported for the silicon-based cross-coupling reactions. The reaction tolerates a wide range of functional groups, including silyl protectors, and allows a gram-scale synthesis to recover and reuse the silicon residue. Copyright
