1217863-66-5 Usage
Description
2-[(3,4-Dimethoxyphenyl)dimethylsilyl]-phenylmethanol is a complex organic chemical compound characterized by its unique molecular structure. It features a phenyl ring with a dimethylsilyl group attached, along with two methoxy groups on the adjacent phenyl ring. The presence of a hydroxyl group classifies it as an alcohol, which contributes to its reactivity and potential applications in various fields.
Uses
Used in Organic Synthesis:
2-[(3,4-Dimethoxyphenyl)dimethylsilyl]-phenylmethanol is utilized as a reagent in organic synthesis due to its distinctive and reactive molecular structure. Its ability to participate in various chemical reactions makes it a valuable component in creating new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-[(3,4-Dimethoxyphenyl)dimethylsilyl]-phenylmethanol may be employed as a building block for the development of novel drugs. Its unique chemical properties could be harnessed to design molecules with specific therapeutic effects, targeting various medical conditions.
Used in Materials Science:
2-[(3,4-Dimethoxyphenyl)dimethylsilyl]-phenylmethanol's structural features also make it potentially useful in materials science, where it could be incorporated into the development of advanced materials with tailored properties. These materials could find applications in a range of industries, from electronics to aerospace engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 1217863-66-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1217863-66:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*6)+(3*3)+(2*6)+(1*6)=165
165 % 10 = 5
So 1217863-66-5 is a valid CAS Registry Number.
1217863-66-5Relevant articles and documents
Copper-mediated transformation of organosilanes to nitriles with DMF and ammonium iodide
Wang, Zhen,Chang, Sukbok
, p. 1990 - 1993 (2013)
Cyanation of aryl-, diaryldimethyl-, and styrylsilanes was developed for the first time under copper-mediated oxidative conditions using ammonium iodide and DMF as the combined source of nitrogen and carbon atom of the introduced cyano unit, respectively. The reaction was observed to proceed in a two-step process: initial conversion of organosilanes to their iodo intermediates and then cyanation. This method has a broad substrate scope with high functional group tolerance.
