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Atomfair 2-(2-Fluoro-5-nitrophenyl)acetic acid C8H6FNO4
Description 2-(2-Fluoro-5-nitrophenyl)acetic acid (CAS No. 195609-18-8) is a high-purity fluorinated nitroaromatic compound with the molecular formula C8H6FNO4. This fine chemical is characterized by its acetic acid functional group attached to a 2-fluoro-5-nitrophenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 199.14 g/mol, this compound is supplied as a crystalline solid with >95% purity (HPLC). Its unique structure enables versatile reactivity, including nucleophilic aromatic substitution and reduction of the nitro group. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. This product is intended for research purposes…
Description
Description
2-(2-Fluoro-5-nitrophenyl)acetic acid (CAS No. 195609-18-8) is a high-purity fluorinated nitroaromatic compound with the molecular formula C8H6FNO4. This fine chemical is characterized by its acetic acid functional group attached to a 2-fluoro-5-nitrophenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 199.14 g/mol, this compound is supplied as a crystalline solid with >95% purity (HPLC). Its unique structure enables versatile reactivity, including nucleophilic aromatic substitution and reduction of the nitro group. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. This product is intended for research purposes only and is not for human or veterinary use.
- CAS No: 195609-18-8
- Molecular Formula: C8H6FNO4
- Molecular Weight: 199.14
- Exact Mass: 199.02808583
- Monoisotopic Mass: 199.02808583
- IUPAC Name: 2-(2-fluoro-5-nitrophenyl)acetic acid
- SMILES: C1=CC(=C(C=C1[N+](=O)[O-])CC(=O)O)F
- Synonyms: 2-(2-fluoro-5-nitrophenyl)acetic acid, 816-003-2, 2-Fluoro-5-nitrophenylacetic acid, 195609-18-8, (2-fluoro-5-nitrophenyl)acetic acid
Application
2-(2-Fluoro-5-nitrophenyl)acetic acid serves as a key building block in medicinal chemistry for the development of novel pharmaceutical compounds. Researchers utilize this compound in the synthesis of fluorinated drug candidates, particularly those targeting inflammatory pathways. The nitro group provides an excellent handle for further functionalization through reduction to amines or conversion to other nitrogen-containing functionalities. In material science, it finds application as a precursor for specialty polymers with unique electronic properties.
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