1-Bromo-5-chloro-3-fluoro-2-iodobenzene

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Reagent Code: #40050
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CAS Number 201849-16-3

science Other reagents with same CAS 201849-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.34 g/mol
Formula C₆H₂BrClFI
badge Registry Numbers
MDL Number MFCD00142591
thermostat Physical Properties
Boiling Point 272°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its unique combination of halogen substituents makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, where it serves as a key intermediate for pharmaceutical and agrochemical development. The presence of multiple halogens allows for selective functionalization, enabling the synthesis of diverse aromatic compounds. Additionally, it is employed in materials science for the preparation of advanced organic materials, including liquid crystals and polymers, due to its ability to introduce specific electronic and steric properties. Its reactivity also makes it useful in the study of halogen bonding interactions in supramolecular chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,268.00
inventory 1g
10-20 days ฿801.00
inventory 10g
10-20 days ฿4,419.00

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1-Bromo-5-chloro-3-fluoro-2-iodobenzene
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This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its unique combination of halogen substituents makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, where it serves as a key intermediate for pharmaceutical and agrochemical development. The presence of multiple halogens allows for selective functionalization, enabling the synthesis of diverse aromatic compounds. Additionally, it is employed in m

This chemical is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its unique combination of halogen substituents makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, where it serves as a key intermediate for pharmaceutical and agrochemical development. The presence of multiple halogens allows for selective functionalization, enabling the synthesis of diverse aromatic compounds. Additionally, it is employed in materials science for the preparation of advanced organic materials, including liquid crystals and polymers, due to its ability to introduce specific electronic and steric properties. Its reactivity also makes it useful in the study of halogen bonding interactions in supramolecular chemistry.

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