1-Bromo-5-chloro-3-fluoro-2-iodobenzene
97%
- Product Code: 40050
CAS:
201849-16-3
| Molecular Weight: | 335.34 g./mol | Molecular Formula: | C₆H₂BrClFI |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00142591 | |
| Melting Point: | Boiling Point: | 272°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $37.62 |
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| 5.000 | 10-20 days | $106.51 |
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| 10.000 | 10-20 days | $207.53 |
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1-Bromo-5-chloro-3-fluoro-2-iodobenzene
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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