2-(2-Bromo-Pyridin-3-YL)-Propan-2-OL

≥97%

Reagent Code: #69837
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CAS Number 909532-39-4

science Other reagents with same CAS 909532-39-4

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Weight 216.08 g/mol
Formula C₈H₁₀BrNO
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the production of more complex compounds. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring a bromine atom and a hydroxyl group, makes it a versatile building block for coupling reactions, such as Suzuki or Heck reactions, which are commonly used to construct biologically active molecules. Additionally, it can be used in agrochemical research for the development of novel pesticides or herbicides, where its pyridine moiety contributes to the biological activity of the final product. Its role in cross-coupling reactions also extends to materials science, where it may be used in the synthesis of organic electronic materials or ligands for catalysis.

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inventory 1g
10-20 days ฿4,920.00

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2-(2-Bromo-Pyridin-3-YL)-Propan-2-OL
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This chemical is primarily utilized in organic synthesis as a key intermediate for the production of more complex compounds. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring a bromine atom and a hydroxyl group, makes it a versatile building block for coupling reactions, such as Suzuki or Heck reactions, which are commonly used to

This chemical is primarily utilized in organic synthesis as a key intermediate for the production of more complex compounds. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of molecules with potential therapeutic applications. Its structure, featuring a bromine atom and a hydroxyl group, makes it a versatile building block for coupling reactions, such as Suzuki or Heck reactions, which are commonly used to construct biologically active molecules. Additionally, it can be used in agrochemical research for the development of novel pesticides or herbicides, where its pyridine moiety contributes to the biological activity of the final product. Its role in cross-coupling reactions also extends to materials science, where it may be used in the synthesis of organic electronic materials or ligands for catalysis.

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