Methyl 3-fluoro-4-iodobenzoate
≥95%
- Product Code: 79407
CAS:
1027513-46-7
| Molecular Weight: | 280.03 g./mol | Molecular Formula: | C₈H₆FIO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09800728 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a building block for more complex molecules. Its structure, featuring both fluorine and iodine substituents, makes it a valuable intermediate in the development of pharmaceuticals and agrochemicals. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are pivotal in creating biologically active compounds. Additionally, the ester group provides a reactive site for hydrolysis or transesterification, enabling the synthesis of various carboxylic acid derivatives or other ester-containing compounds. Its applications are particularly significant in medicinal chemistry, where it can be used to design and synthesize drug candidates with specific target interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿603.00 |
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| 0.250 | 10-20 days | ฿1,224.00 |
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Methyl 3-fluoro-4-iodobenzoate
This compound is primarily utilized in organic synthesis as a building block for more complex molecules. Its structure, featuring both fluorine and iodine substituents, makes it a valuable intermediate in the development of pharmaceuticals and agrochemicals. The presence of the iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are pivotal in creating biologically active compounds. Additionally, the ester group provides a reactive site for hydrolysis or transesterification, enabling the synthesis of various carboxylic acid derivatives or other ester-containing compounds. Its applications are particularly significant in medicinal chemistry, where it can be used to design and synthesize drug candidates with specific target interactions.
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