1-Bromo-3-iodo-5-nitrobenzene

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Reagent Code: #59527
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CAS Number 861601-15-2

science Other reagents with same CAS 861601-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.90 g/mol
Formula C₆H₃BrINO₂
badge Registry Numbers
MDL Number MFCD13194576
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

description Product Description

Used in organic synthesis as a versatile intermediate for creating complex molecules, particularly in pharmaceuticals and agrochemicals. Its halogen substituents (bromo and iodo) allow for selective cross-coupling reactions, such as Suzuki or Sonogashira reactions, to build aromatic compounds. The nitro group enhances reactivity, making it valuable for further functionalization, including reduction to amines or substitution reactions. It is also employed in material science for designing organic electronic materials or dyes due to its electron-withdrawing properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,700.00
inventory 250mg
10-20 days ฿666.00
inventory 1g
10-20 days ฿2,610.00

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1-Bromo-3-iodo-5-nitrobenzene
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Used in organic synthesis as a versatile intermediate for creating complex molecules, particularly in pharmaceuticals and agrochemicals. Its halogen substituents (bromo and iodo) allow for selective cross-coupling reactions, such as Suzuki or Sonogashira reactions, to build aromatic compounds. The nitro group enhances reactivity, making it valuable for further functionalization, including reduction to amines or substitution reactions. It is also employed in material science for designing organic electron

Used in organic synthesis as a versatile intermediate for creating complex molecules, particularly in pharmaceuticals and agrochemicals. Its halogen substituents (bromo and iodo) allow for selective cross-coupling reactions, such as Suzuki or Sonogashira reactions, to build aromatic compounds. The nitro group enhances reactivity, making it valuable for further functionalization, including reduction to amines or substitution reactions. It is also employed in material science for designing organic electronic materials or dyes due to its electron-withdrawing properties.

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