217469-85-7 Usage
Description
(2-(2-bromo-phenyl)ethynyl)triethylsilane is a chemical compound with the molecular formula C17H21BrSi. It is a silane compound that contains a triethylsilyl group and an ethynyl group attached to a phenyl ring with a bromine substitution at the 2-position.
Uses
Used in Organic Synthesis:
(2-(2-bromo-phenyl)ethynyl)triethylsilane is used as a building block in organic synthesis for the preparation of functionalized silanes and as a precursor in the production of silicon-based materials.
Used in Cross-coupling Reactions:
(2-(2-bromo-phenyl)ethynyl)triethylsilane is used as a reactant in cross-coupling reactions to form carbon-carbon and carbon-heteroatom bonds.
Used in Materials Science:
(2-(2-bromo-phenyl)ethynyl)triethylsilane has potential applications in the field of materials science for the development of new materials with unique properties.
Used in Pharmaceuticals:
(2-(2-bromo-phenyl)ethynyl)triethylsilane has potential applications in the pharmaceutical industry for the synthesis of new drug molecules.
Used in Agrochemicals:
(2-(2-bromo-phenyl)ethynyl)triethylsilane has potential applications in the agrochemical industry for the development of new pesticides and other agricultural chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 217469-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,4,6 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 217469-85:
(8*2)+(7*1)+(6*7)+(5*4)+(4*6)+(3*9)+(2*8)+(1*5)=157
157 % 10 = 7
So 217469-85-7 is a valid CAS Registry Number.
217469-85-7Relevant articles and documents
Visible light-promoted radical cyclization of silicon-tethered alkyl iodide and phenyl alkyne. An efficient approach to synthesize benzosilolines
Lin, Xinglong,Gan, Zubao,Lu, Ji,Su, Zhishan,Hu, Changwei,Zhang, Yuebao,Wu, Ya,Gao, Lu,Song, Zhenlei
, p. 6189 - 6192 (2016)
An efficient approach to synthesize benzosiloline has been developed using a visible light-promoted radical cyclization reaction of silicon-tethered alkyl iodide and phenyl alkyne.
