3,5-Difluorocinnamic acid is an organic compound characterized by the presence of two fluorine atoms located at the 3 and 5 positions of the cinnamic acid structure. It features a trans configuration, which is significant for its stability and reactivity. The compound has a carboxylic acid functional group, contributing to its acidity and potential for forming hydrogen bonds. 3,5-Difluorocinnamic acid is typically a white to off-white solid at room temperature and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water due to its hydrophobic aromatic system. The presence of fluorine atoms enhances its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry and material science. Additionally, this compound may exhibit unique optical properties and reactivity patterns, which can be exploited in various synthetic applications. Its CAS number, 84315-23-1, is a unique identifier that facilitates its recognition in chemical databases and literature.

3,5-Difluorocinnamic acid

84315-23-1: 2-Propenoic Acid, 3-(3,5-Difluorophenyl)-, 3-(3,5-Difluorophenyl)acrylic acid, 3-(3,5-Difluorophenyl)Prop-2-Enoic Acid

3-(3,5-Difluorophenyl)acrylic acid

3,5-Difluorocinnamic Acid is a synthetic monomer that can be used to prepare a variety of organic compounds. The synthesis of 3,5-difluorocinnamic acid can be achieved by electrochemical methods in the presence of an electrolyte (e.g., KOH) and radiation (e.g., UV light), or by reacting phenylacetic acid with fluorine gas in the presence of an inorganic base (e.g., potassium fluoride). This molecule has two orientations, which are cis and trans. The molecular formula for 3,5-difluorocinnamic acid is C9H6F2O3.

CAS 84315-23-1: 3,5-Difluorocinnamic acid

3-(3,5-Difluorophenyl)acrylic acid

Ref: 10-F980254

3,5-difluorocinnamic Acid

Ref: 3D-FD105088

3-(3,5-Difluorophenyl)acrylic acid

Ref: IN-DA003IMX