Methyl 5-chloro-2-methoxy-4-(N-methylacetamido)benzoate
95%
- Product Code: 83816
CAS:
202822-76-2
| Molecular Weight: | 271.70 g./mol | Molecular Formula: | C₁₂H₁₄ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31802700 | |
| Melting Point: | 105.5-107 °C | Boiling Point: | 403.8±45.0 °C(Predicted) |
| Density: | 1.264±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound 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 chloro and methoxy groups, makes it a versatile building block for constructing pharmaceuticals, particularly those targeting specific biological pathways.
In medicinal chemistry, it is often employed in the development of anti-inflammatory and analgesic agents due to its ability to interact with enzymes and receptors involved in pain and inflammation. Additionally, its acetamido group can be modified to enhance drug bioavailability and stability, making it valuable in drug design and optimization processes.
Furthermore, it finds application in agrochemical research, where it is used to synthesize compounds with potential herbicidal or pesticidal properties. Its chemical framework allows for the creation of derivatives that can target specific pests or weeds, contributing to the development of more effective and environmentally friendly agricultural solutions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | €24.69 |
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| 5.000 | 10-20 days | €74.08 |
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| 25.000 | 10-20 days | €265.46 |
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Methyl 5-chloro-2-methoxy-4-(N-methylacetamido)benzoate
This compound 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 chloro and methoxy groups, makes it a versatile building block for constructing pharmaceuticals, particularly those targeting specific biological pathways.
In medicinal chemistry, it is often employed in the development of anti-inflammatory and analgesic agents due to its ability to interact with enzymes and receptors involved in pain and inflammation. Additionally, its acetamido group can be modified to enhance drug bioavailability and stability, making it valuable in drug design and optimization processes.
Furthermore, it finds application in agrochemical research, where it is used to synthesize compounds with potential herbicidal or pesticidal properties. Its chemical framework allows for the creation of derivatives that can target specific pests or weeds, contributing to the development of more effective and environmentally friendly agricultural solutions.
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