N,N-Diethyl-4-fluoro-3-nitrobenzamide
97%
- Product Code: 121294
CAS:
474018-94-5
| Molecular Weight: | 240.23 g./mol | Molecular Formula: | C₁₁H₁₃FN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12408749 | |
| Melting Point: | Boiling Point: | 390.1±32.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
N,N-Diethyl-4-fluoro-3-nitrobenzamide is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical compounds. Its structure, featuring a nitro group and a fluorine atom, makes it a valuable precursor in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require specific aromatic substitutions. Additionally, it is employed in research settings for studying chemical reactions involving nitroaromatic compounds, which are often explored for their potential applications in medicinal chemistry and material science. The compound’s unique properties also make it suitable for use in the development of agrochemicals, where its derivatives may exhibit herbicidal or pesticidal activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,341.00 |
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| 0.250 | 10-20 days | ฿2,682.00 |
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N,N-Diethyl-4-fluoro-3-nitrobenzamide
N,N-Diethyl-4-fluoro-3-nitrobenzamide is primarily utilized in the field of organic synthesis as an intermediate for the development of more complex chemical compounds. Its structure, featuring a nitro group and a fluorine atom, makes it a valuable precursor in the synthesis of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs) that require specific aromatic substitutions. Additionally, it is employed in research settings for studying chemical reactions involving nitroaromatic compounds, which are often explored for their potential applications in medicinal chemistry and material science. The compound’s unique properties also make it suitable for use in the development of agrochemicals, where its derivatives may exhibit herbicidal or pesticidal activities.
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