2,3,5,6-tetrafluoro-4-iodobenzaldehyde
98%
- Product Code: 238934
CAS:
837368-26-0
| Molecular Weight: | 303.98 g./mol | Molecular Formula: | C₇HIF₄O |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8 °C, sealed, dry |
Product Description:
Used primarily as a building block in the synthesis of advanced organic compounds, especially in pharmaceuticals and agrochemicals. Its unique structure with multiple fluorine atoms and an iodine substituent makes it valuable in medicinal chemistry for modifying drug potency and metabolic stability. The aldehyde group allows for easy functionalization, enabling coupling reactions such as Wittig or reductive amination to form more complex molecules. It is also employed in materials science, particularly in the development of fluorinated liquid crystals and organic electronic materials, where fluorine substitution enhances thermal and oxidative stability. The iodine moiety facilitates cross-coupling reactions like Suzuki or Heck reactions, expanding its utility in creating biaryl systems for functional molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | €293.84 |
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| 250mg | 10-20 days | €587.14 |
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| 1g | 10-20 days | €1,549.82 |
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| bulk | 10-20 days | €0.00 |
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2,3,5,6-tetrafluoro-4-iodobenzaldehyde
Used primarily as a building block in the synthesis of advanced organic compounds, especially in pharmaceuticals and agrochemicals. Its unique structure with multiple fluorine atoms and an iodine substituent makes it valuable in medicinal chemistry for modifying drug potency and metabolic stability. The aldehyde group allows for easy functionalization, enabling coupling reactions such as Wittig or reductive amination to form more complex molecules. It is also employed in materials science, particularly in the development of fluorinated liquid crystals and organic electronic materials, where fluorine substitution enhances thermal and oxidative stability. The iodine moiety facilitates cross-coupling reactions like Suzuki or Heck reactions, expanding its utility in creating biaryl systems for functional molecules.
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