4-(Benzyloxy)-2-bromo-1-fluorobenzene

97%

Reagent Code: #87456
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CAS Number 1364572-05-3

science Other reagents with same CAS 1364572-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.12 g/mol
Formula C₁₃H₁₀BrFO
badge Registry Numbers
MDL Number MFCD25320165
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block in pharmaceutical and agrochemical research. The benzyloxy group provides a protective functionality, allowing selective reactions to occur at other sites of the molecule. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl or aryl-heteroaryl compounds. These reactions are crucial in developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogenated aromatic ring makes it suitable for further functionalization, enabling the synthesis of diverse chemical entities with potential biological or industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,478.00
inventory 100mg
10-20 days ฿4,995.00
inventory 1g
10-20 days ฿22,878.00

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4-(Benzyloxy)-2-bromo-1-fluorobenzene
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This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block in pharmaceutical and agrochemical research. The benzyloxy group provides a protective functionality, allowing selective reactions to occur at other sites of the molecule. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl or aryl-het

This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block in pharmaceutical and agrochemical research. The benzyloxy group provides a protective functionality, allowing selective reactions to occur at other sites of the molecule. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl or aryl-heteroaryl compounds. These reactions are crucial in developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogenated aromatic ring makes it suitable for further functionalization, enabling the synthesis of diverse chemical entities with potential biological or industrial applications.

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