(E)-3-(4-Fluoro-phenyl)-but-2-enoic acid, commonly referred to as a substituted cinnamic acid derivative, is characterized by its unique structural features, including a double bond between the second and third carbon atoms of the butenoic acid chain and a fluorinated phenyl group at the 3-position. This compound exhibits both acidic and aromatic properties, making it relevant in various chemical and pharmaceutical applications. The presence of the fluorine atom enhances its lipophilicity and may influence its biological activity, potentially affecting its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity can be attributed to the double bond, which can participate in various chemical reactions, such as electrophilic addition or polymerization. Additionally, the compound's stereochemistry, indicated by the (E) configuration, suggests that the substituents on either side of the double bond are on opposite sides, which can influence its physical and chemical properties, including its melting point and reactivity.

(E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID

1201-86-1: (E)-3-(4-Fluoro-phenyl)-but-2-enoic acid, commonly referred to as a substituted cinnamic acid derivative, is characterized by its unique structural features, including a double bond between the second and third carbon atoms of the butenoic acid chain and a fluorinated phenyl group at the 3-position. This compound exhibits both acidic and aromatic properties, making it relevant in various chemical and pharmaceutical applications. The presence of the fluorine atom enhances its lipophilicity and may influence its biological activity, potentially affecting its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity can be attributed to the double bond, which can participate in various chemical reactions, such as electrophilic addition or polymerization. Additionally, the compound's stereochemistry, indicated by the (E) configuration, suggests that the substituents on either side of the double bond are on opposite sides, which can influence its physical and chemical properties, including its melting point and reactivity.

3-(4-Fluorophenyl)but-2-enoic acid

<p>(2E)-3-(4-Fluorophenyl)but-2-enoic acid</p>

(2E)-3-(4-Fluorophenyl)but-2-enoic acid

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CAS 1201-86-1

(E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID

3-(4-Fluorophenyl)but-2-enoic acid

Ref: IN-DA000QAU

(2E)-3-(4-Fluorophenyl)but-2-enoic acid

Ref: 54-PC106108

(2E)-3-(4-Fluorophenyl)-2-Butenoic Acid

Ref: 3D-FF84767