17048-07-6 Usage
Uses
Used in Organic Synthesis:
(2-bromo-3,4,5,6-tetrafluorophenyl)(trimethyl)silane is used as a reagent for the formation of carbon-silicon bonds in organic synthesis. Its reactivity allows for the creation of various organic compounds, making it a valuable component in the synthesis process.
Used in Specialty Chemicals Production:
(2-bromo-3,4,5,6-tetrafluorophenyl)(trimethyl)silane is utilized in the production of specialty chemicals, where its unique properties contribute to the development of specific chemical products with tailored characteristics.
Used in Pharmaceutical Industry:
(2-bromo-3,4,5,6-tetrafluorophenyl)(trimethyl)silane is also used in the pharmaceutical industry, where it serves as a cross-coupling reagent in the synthesis of various organic compounds with potential medicinal applications.
Safety Note:
Due to its reactivity and potential hazards, proper handling and storage procedures should be followed when working with (2-bromo-3,4,5,6-tetrafluorophenyl)(trimethyl)silane to ensure safety and prevent accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 17048-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,4 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17048-07:
(7*1)+(6*7)+(5*0)+(4*4)+(3*8)+(2*0)+(1*7)=96
96 % 10 = 6
So 17048-07-6 is a valid CAS Registry Number.
17048-07-6Relevant academic research and scientific papers
Reactions of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino)phosphine: 6. * Reactions of halogenotetrafluorobenzenes RC6F4X (X = Cl, Br, or I) with chlorotrimethylsilane
Bardin
, p. 780 - 785 (2007/10/03)
The rate of replacement of the halogen atom in isomers of RC6F4X (X = Cl, Br, or I) by the SiMe3 group under the action of Me3SiCl and P(NEt2)3 depends on the nature and the mutual arrangement of the substituents X and R. In addition to silyldehalogenation, compounds C6HF4X (X = Br or I) undergo silyldeprotonation and reduction to tetrafluorobenzenes.
