Methyl 4-bromo-2,3-difluoro-5-iodobenzoate
95%
- Product Code: 83949
CAS:
1878217-46-9
Molecular Weight: | 376.92 g./mol | Molecular Formula: | C₈H₄BrF₂IO₂ |
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EC Number: | MDL Number: | MFCD31652390 | |
Melting Point: | Boiling Point: | 360.4±42.0 °C(Predicted) | |
Density: | 2.166±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its unique structure, featuring multiple halogen substituents, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of bromo, fluoro, and iodo groups allows for selective functionalization through various cross-coupling reactions, such as Suzuki or Sonogashira reactions, enabling the creation of diverse aromatic compounds. Additionally, it can be employed in the synthesis of liquid crystals and organic electronic materials, where precise halogen substitution patterns are critical for tuning material properties. Its ester group also provides a handle for further chemical modifications, enhancing its versatility in synthetic applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿8,199.00 |
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0.250 | 10-20 days | ฿14,580.00 |
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1.000 | 10-20 days | ฿29,160.00 |
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Methyl 4-bromo-2,3-difluoro-5-iodobenzoate
This compound is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its unique structure, featuring multiple halogen substituents, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of bromo, fluoro, and iodo groups allows for selective functionalization through various cross-coupling reactions, such as Suzuki or Sonogashira reactions, enabling the creation of diverse aromatic compounds. Additionally, it can be employed in the synthesis of liquid crystals and organic electronic materials, where precise halogen substitution patterns are critical for tuning material properties. Its ester group also provides a handle for further chemical modifications, enhancing its versatility in synthetic applications.
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