CAS 199664-70-5

5-(2-fluorophenyl)-5-oxo-pentanoic acid

Description:

5-(2-Fluorophenyl)-5-oxo-pentanoic acid, with the CAS number 199664-70-5, is an organic compound characterized by its unique structure that includes a pentanoic acid backbone substituted with a 2-fluorophenyl group and a ketone functional group. This compound typically exhibits properties associated with both carboxylic acids and ketones, such as acidity due to the carboxylic acid group and potential reactivity from the carbonyl group. The presence of the fluorine atom in the phenyl ring can influence the compound's electronic properties, potentially enhancing its lipophilicity and altering its biological activity. It may be used in various chemical syntheses or as an intermediate in pharmaceutical development. The compound's solubility, stability, and reactivity can vary based on environmental conditions such as pH and temperature. As with many organic compounds, safety data sheets should be consulted for handling and storage guidelines, as well as potential hazards associated with its use.

Formula: C₁₁H₁₁FO₃

InChI: InChI=1/C11H11FO3/c12-9-5-2-1-4-8(9)10(13)6-3-7-11(14)15/h1-2,4-5H,3,6-7H2,(H,14,15)

SMILES: c1ccc(c(c1)C(=O)CCCC(=O)O)F

Synonyms:

• 5-(2-fluorophenyl)-5-oxopentanoicaci
• Ezetimibe Impurity 97
• Benzenepentanoic acid, 2-fluoro-δ-oxo-
• 5-(2-fluorophenyl)-5-oxopentanoic acid
• 5-(2-FLUOROPHENYL)-5-OXOVALERIC ACID
• Ezetimibe Impuriry 47

Benzenepentanoic acid, 2-fluoro-δ-oxo-

CAS: 199664-70-5

Formula: C₁₁H₁₁FO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 210.2016

Ref: IN-DA002C9X

5-(2-Fluorophenyl)-5-oxopentanoic acid

CAS: 199664-70-5

5-(2-Fluorophenyl)-5-oxopentanoic acid

Purity: 95%

Molecular weight: 210.2g/mol

Ref: 54-PC1003658

5-(2-Fluorophenyl)-5-oxovaleric Acid

Controlled Product

CAS: 199664-70-5

Applications 5-(2-Fluorophenyl)-5-oxovaleric Acid is used as a reagent in the preparation of indole derivatives which act as cell protective agents. It is also used as a reagent in the catalytic N-nitroso aldol reaction of γ,δ-unsaturated δ-lactones.
References Yamamoto, I., et al.: Preparation of indole derivatives as cell protective agents, WO Patent 9745410, Dec 4, 1997; Yanagisawa, A., et al.: Org. Lett., 14, 2434 (2012);

Formula: C₁₁H₁₁FO₃

Color and Shape: Neat

Molecular weight: 210.2

Ref: TR-F489595

5-(2-Fluorophenyl)-5-Oxopentanoic Acid

CAS: 199664-70-5

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Formula: C₁₁H₁₁FO₃

Purity: Min. 95%

Molecular weight: 210.2 g/mol

Ref: 3D-FF84429

Ezetimibe Impurity 47

CAS: 199664-70-5

Formula: C₁₁H₁₁FO₃

Molecular weight: 210.2

Ref: ST-EA-CP-E6088