4-Amino-2,3-difluoro-5-nitrobenzoic acid
≥95%
- Product Code: 118995
CAS:
284030-57-5
| Molecular Weight: | 218.11 g./mol | Molecular Formula: | C₇H₄F₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08543937 | |
| Melting Point: | Boiling Point: | 401.139°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) due to its unique structure, which allows for further functionalization. The presence of amino, nitro, and carboxylic acid groups makes it a versatile building block for creating compounds with potential biological activity. It is often employed in the preparation of fluorinated aromatic compounds, which are of significant interest in drug discovery for their enhanced stability and bioavailability. Additionally, its nitro group can be reduced to form amines, enabling the creation of diverse chemical structures for screening in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿603.00 |
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| 5.000 | 10-20 days | ฿2,106.00 |
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| 10.000 | 10-20 days | ฿3,600.00 |
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4-Amino-2,3-difluoro-5-nitrobenzoic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) due to its unique structure, which allows for further functionalization. The presence of amino, nitro, and carboxylic acid groups makes it a versatile building block for creating compounds with potential biological activity. It is often employed in the preparation of fluorinated aromatic compounds, which are of significant interest in drug discovery for their enhanced stability and bioavailability. Additionally, its nitro group can be reduced to form amines, enabling the creation of diverse chemical structures for screening in medicinal chemistry.
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