17021-92-0 Usage
Uses
Used in Chemical Synthesis:
(4-bromophenyl)(methoxy)dimethylsilane is used as a key intermediate in the synthesis of organic and organometallic compounds. Its unique structure allows for the formation of new chemical bonds and the creation of complex molecules.
Used in Specialty Chemicals Production:
(4-bromophenyl)(methoxy)dimethylsilane is utilized in the production of specialty chemicals, which are high-value chemicals used in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Development:
(4-bromophenyl)(methoxy)dimethylsilane is used as a reactant in the preparation of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
It is also employed in the production of agrochemicals, such as pesticides and fertilizers, to improve agricultural productivity and crop protection.
Used in Materials and Coatings Development:
Due to its unique chemical and physical properties, (4-bromophenyl)(methoxy)dimethylsilane has potential applications in the development of advanced materials and coatings, which can be used in various industries, including automotive, aerospace, and construction.
Check Digit Verification of cas no
The CAS Registry Mumber 17021-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17021-92:
(7*1)+(6*7)+(5*0)+(4*2)+(3*1)+(2*9)+(1*2)=80
80 % 10 = 0
So 17021-92-0 is a valid CAS Registry Number.
17021-92-0Relevant academic research and scientific papers
Synthesis of phenols via fluoride-free oxidation of arylsilanes and arylmethoxysilanes
Rayment, Elizabeth J.,Summerhill, Nick,Anderson, Edward A.
, p. 7052 - 7060 (2012/10/07)
Rapid, efficient methods have been developed to prepare phenols from the oxidation of arylhydrosilanes. The effects of arene substituents and fluoride promoters on this process show that while electron-deficient arenes can undergo direct oxidation from the hydrosilane, electron-rich aromatics benefit from silane activation via oxidation to the methoxysilane using homogeneous or heterogeneous transition metal catalysis. The combination of these two oxidations into a streamlined flow procedure involving minimal processing of reaction intermediates is also reported.
