127406-53-5

Basic information

• Product Name: (E)-4-(2-fluorophenyl)but-3-enoic acid
• Synonyms: (E)-4-(2-fluorophenyl)but-3-enoic acid;4-(2-Fluoro-phenyl)-but-3-enoic acid
• CAS NO: 127406-53-5
• Molecular Formula: C10H9FO2
• Molecular Weight: 180.1756632
• Mol File: 127406-53-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-4-(2-fluorophenyl)but-3-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-(2-fluorophenyl)but-3-enoic acid(127406-53-5)
• EPA Substance Registry System: (E)-4-(2-fluorophenyl)but-3-enoic acid(127406-53-5)

Safety Data

• Hazardous Substances Data: 127406-53-5(Hazardous Substances Data)

Usage

Description

(E)-4-(2-fluorophenyl)but-3-enoic acid is a chemical compound characterized by the molecular formula C10H9FO2. It is a carboxylic acid featuring a but-3-enoic acid functional group and a 2-fluorophenyl substituent. (E)-4-(2-fluorophenyl)but-3-enoic acid is known for its potential pharmacological properties and is widely utilized in organic synthesis and pharmaceutical research due to its unique molecular structure and chemical characteristics.

Uses

Used in Pharmaceutical Research:
(E)-4-(2-fluorophenyl)but-3-enoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential pharmacological properties. Its molecular structure allows for the development of new drugs with improved efficacy and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-4-(2-fluorophenyl)but-3-enoic acid serves as a valuable building block for creating a range of complex organic molecules. Its reactivity and functional groups make it a versatile compound for constructing novel chemical entities.
Used in Material Science:
(E)-4-(2-fluorophenyl)but-3-enoic acid may also find applications in the development of new materials, thanks to its unique chemical structure. Its properties could contribute to the creation of advanced materials with specific characteristics, such as improved strength, durability, or chemical resistance.
Used as a Reagent in Organic Reactions:
Furthermore, (E)-4-(2-fluorophenyl)but-3-enoic acid can be employed as a reagent in various organic reactions, facilitating the formation of new chemical bonds and aiding in the synthesis of a wide array of organic compounds.