2-Fluoro-4-nitrophenylacetonitrile
≥98%
- Product Code: 80821
CAS:
853910-00-6
Molecular Weight: | 180.14 g./mol | Molecular Formula: | C₈H₅FN₂O₂ |
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Density: | Storage Condition: | room temperature, dry |
Product Description:
2-Fluoro-4-nitrophenylacetonitrile is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both a nitrile group and a nitro group, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The compound is often employed in the preparation of active pharmaceutical ingredients (APIs) where the nitrile group can be further transformed into various functional groups such as amines, carboxylic acids, or amides. Additionally, the presence of the nitro group allows for further chemical modifications, including reductions to amines or participation in nucleophilic aromatic substitution reactions. This chemical is also used in research settings for the development of novel organic molecules with potential biological activity, making it a key building block in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $103.16 |
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2-Fluoro-4-nitrophenylacetonitrile
2-Fluoro-4-nitrophenylacetonitrile is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both a nitrile group and a nitro group, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The compound is often employed in the preparation of active pharmaceutical ingredients (APIs) where the nitrile group can be further transformed into various functional groups such as amines, carboxylic acids, or amides. Additionally, the presence of the nitro group allows for further chemical modifications, including reductions to amines or participation in nucleophilic aromatic substitution reactions. This chemical is also used in research settings for the development of novel organic molecules with potential biological activity, making it a key building block in medicinal chemistry and drug discovery processes.
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