Methyl 4-acetamido-5-iodo-2-methoxybenzoate
≥95%
- Product Code: 118838
CAS:
201214-53-1
| Molecular Weight: | 349.12 g./mol | Molecular Formula: | C₁₁H₁₂INO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13192093 | |
| Melting Point: | Boiling Point: | 474.802°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both an acetamido and an iodo group, makes it particularly valuable in the construction of pharmaceuticals and bioactive compounds.
In medicinal chemistry, it is often employed in the development of drugs targeting specific biological pathways, especially those involving iodine-containing compounds. The presence of the methoxy group enhances its reactivity, allowing for further functionalization and modification in synthetic routes.
Additionally, it finds application in research settings as a building block for the synthesis of novel organic materials. Its unique properties make it suitable for studies aimed at understanding chemical reactivity and designing new molecules with potential industrial or therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿963.00 |
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| 0.250 | 10-20 days | ฿1,449.00 |
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| 1.000 | 10-20 days | ฿3,609.00 |
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Methyl 4-acetamido-5-iodo-2-methoxybenzoate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both an acetamido and an iodo group, makes it particularly valuable in the construction of pharmaceuticals and bioactive compounds.
In medicinal chemistry, it is often employed in the development of drugs targeting specific biological pathways, especially those involving iodine-containing compounds. The presence of the methoxy group enhances its reactivity, allowing for further functionalization and modification in synthetic routes.
Additionally, it finds application in research settings as a building block for the synthesis of novel organic materials. Its unique properties make it suitable for studies aimed at understanding chemical reactivity and designing new molecules with potential industrial or therapeutic applications.
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