CAS 399-31-5
:2′-Fluoroacetanilide
Description:
2′-Fluoroacetanilide, with the CAS number 399-31-5, is an organic compound that belongs to the class of acetanilides. It features a fluorine atom substituted at the para position of the aniline ring, which influences its chemical properties and reactivity. This compound typically appears as a white to off-white crystalline solid and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water. The presence of the fluorine atom enhances its lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry. 2′-Fluoroacetanilide can participate in various chemical reactions, including nucleophilic substitutions and acylation reactions, due to the presence of both the acetamide and aromatic functionalities. Its derivatives may exhibit diverse pharmacological properties, contributing to its relevance in drug development and synthesis. As with many chemical substances, proper handling and safety measures should be observed due to potential toxicity and environmental impact.
Formula:C8H8FNO
InChI:InChI=1S/C8H8FNO/c1-6(11)10-8-5-3-2-4-7(8)9/h2-5H,1H3,(H,10,11)
InChI key:InChIKey=AUZPZBPZWHEIDY-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(F)C=CC=C1
Synonyms:- Acetamide, N-(2-fluorophenyl)-
- Acetanilide, 2′-fluoro-
- N-(2-Fluorophenyl)acetamide
- N-cyclohexyl-2-fluoroacetamide
- NSC 51783
- o-Fluoroacetanilide
- 2'-Fluoroacetanilide
- 2′-Fluoroacetanilide
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Found 6 products.
2'-Fluoroacetanilide
CAS:Formula:C8H8FNOPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:153.16N-(2-fluorophenyl)acetamide
CAS:Formula:C8H8FNOPurity:98%Color and Shape:SolidMolecular weight:153.15362'-Fluoroacetanilide
CAS:2'-FluoroacetanilideFormula:C8H8FNOPurity:98%Color and Shape: beige solidMolecular weight:153.15g/mol2-Fluoroacetanilide
CAS:<p>2-Fluoroacetanilide is an organic compound that is used as a building block in organic synthesis. It has been shown to be an optimal substrate for the reaction with carbon disulfide and wild-type virus, which are both proteins. The use of rat liver microsomes as a model system has allowed for the study of 2-fluoroacetanilide's effect on the metabolism of other drugs. 2-Fluoroacetanilide is also soluble in water and shows thermal expansion properties. 2-Fluoroacetanilide has been shown to react with ammonium hydroxide to form quinoxalines, which are compounds that have been studied as potential antiviral agents. This compound's chemical structure includes fluorine, which can be found in its NMR spectra and hydrochloric acid.br>br><br>2-Fluoroacetanilide is not active against influenza virus, but it has been shown to</p>Formula:C8H8FNOPurity:Min. 95%Color and Shape:PowderMolecular weight:153.15 g/mol





