Methyl 4-iodo-2-methoxybenzoate
98%
- Product Code: 211348
CAS:
148490-97-5
| Molecular Weight: | 292.07 g./mol | Molecular Formula: | C₉H₉IO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797865 | |
| Melting Point: | 44-46 °C | Boiling Point: | 332.7 °C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, dry, light-proof |
Product Description:
Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ester and methoxy groups provide sites for further functionalization, making it valuable in the development of bioactive molecules. Commonly employed in the preparation of analgesic and anti-inflammatory compounds due to its structural similarity to known active scaffolds. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,110.00 |
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| 5g | 10-20 days | ฿3,700.00 |
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| 25g | 10-20 days | ฿15,110.00 |
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Methyl 4-iodo-2-methoxybenzoate
Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. The iodine substituent allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ester and methoxy groups provide sites for further functionalization, making it valuable in the development of bioactive molecules. Commonly employed in the preparation of analgesic and anti-inflammatory compounds due to its structural similarity to known active scaffolds. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies.
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