2-bromo-6-(2-((tert-butyldimethylsilyl)oxy)ethyl)pyridine

Reagent Code: #142317
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CAS Number 2378097-35-7

science Other reagents with same CAS 2378097-35-7

blur_circular Chemical Specifications

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Weight 316.313 g/mol
Formula C₁₃H₂₂BrNOSi
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The silyl-protected hydroxyethyl group provides a handle for further modification, where deprotection yields a free alcohol for additional derivatization. Commonly employed in the synthesis of bioactive compounds, including potential drug candidates targeting neurological and inflammatory conditions. Its structure supports the development of pyridine-based derivatives with tailored pharmacological properties.

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inventory 1g
10-20 days ฿22,800.00

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2-bromo-6-(2-((tert-butyldimethylsilyl)oxy)ethyl)pyridine
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The silyl-protected hydroxyethyl group provides a handle for further modification, where deprotection yields a free alcohol for additional derivatization. Commonly employed in the synthesis of bioactive compounds, including potential drug

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The silyl-protected hydroxyethyl group provides a handle for further modification, where deprotection yields a free alcohol for additional derivatization. Commonly employed in the synthesis of bioactive compounds, including potential drug candidates targeting neurological and inflammatory conditions. Its structure supports the development of pyridine-based derivatives with tailored pharmacological properties.

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