1,3-Difluoro-5-iodo-2-methoxybenzene
95%
- Product Code: 38914
CAS:
886762-68-1
| Molecular Weight: | 270.0153 g./mol | Molecular Formula: | C₇H₅F₂IO |
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| EC Number: | MDL Number: | MFCD07368787 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its unique structure, featuring fluorine and iodine substituents, makes it a suitable candidate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating diverse organic compounds. Additionally, it is employed in material science for the design of advanced materials, including liquid crystals and polymers, due to its ability to impart specific electronic and structural properties. Its methoxy group also enhances its reactivity in various chemical transformations, making it a versatile reagent in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿819.00 |
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1,3-Difluoro-5-iodo-2-methoxybenzene
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its unique structure, featuring fluorine and iodine substituents, makes it a suitable candidate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating diverse organic compounds. Additionally, it is employed in material science for the design of advanced materials, including liquid crystals and polymers, due to its ability to impart specific electronic and structural properties. Its methoxy group also enhances its reactivity in various chemical transformations, making it a versatile reagent in synthetic chemistry.
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