((4-Bromo-3-fluorobenzyl)oxy)(tert-butyl)dimethylsilane

98%

Reagent Code: #129861
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CAS Number 1017598-60-5

science Other reagents with same CAS 1017598-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.29 g/mol
Formula C₁₃H₂₀BrFOSi
badge Registry Numbers
MDL Number MFCD31802578
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated and brominated aromatic molecules. Its silyl ether functionality acts as a protecting group for alcohols during multi-step organic syntheses, allowing selective reactions at other sites in the molecule. The presence of both bromo and fluoro substituents enables further functionalization through cross-coupling reactions, such as Suzuki or Ullmann couplings, making it valuable in medicinal chemistry for building complex drug-like structures. Commonly employed in research settings for the preparation of bioactive molecules and potential therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,480.00
inventory 1g
10-20 days ฿3,990.00

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((4-Bromo-3-fluorobenzyl)oxy)(tert-butyl)dimethylsilane
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated and brominated aromatic molecules. Its silyl ether functionality acts as a protecting group for alcohols during multi-step organic syntheses, allowing selective reactions at other sites in the molecule. The presence of both bromo and fluoro substituents enables further functionalization through cross-coupling reactions, such as Suzuki or Ullmann couplings, making it valuable in medicinal c

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated and brominated aromatic molecules. Its silyl ether functionality acts as a protecting group for alcohols during multi-step organic syntheses, allowing selective reactions at other sites in the molecule. The presence of both bromo and fluoro substituents enables further functionalization through cross-coupling reactions, such as Suzuki or Ullmann couplings, making it valuable in medicinal chemistry for building complex drug-like structures. Commonly employed in research settings for the preparation of bioactive molecules and potential therapeutic agents.

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