| product_name | (2E)-3-(2,5-Difluorophenyl)acrylic acid, trans-3-(2,5-Difluorophenyl)prop-2-enoic acid |
| CAS_number | 173495-54-6 |
| formula | C9H6F2O2 |
| molar_mass | 184.14 g/mol |
| density | 1.35 g/cm³ |
| boiling_point | 291 °C |
| melting_point | 145-148 °C |
| solubility_in_water | Slightly soluble |
| pKa | 4.56 |
| flash_point | 129 °C |
| appearance | White to off-white powder |
| refractive_index | 1.518 |
| logP | 2.1 |
| stability | Stable under standard conditions |
| storage_conditions | Store in a cool, dry place |
What are the key features of (2E)-3-(2,5-Difluorophenyl)acrylic acid, trans-3-(2,5-Difluorophenyl)prop-2-enoic acid?
(2E)-3-(2,5-Difluorophenyl)acrylic acid, trans-3-(2,5-Difluorophenyl)prop-2-enoic acid is a compound that belongs to the class of organic compounds known as phenylpropanoic acids. It is characterized by its 2,5-difluorophenyl substitution on the acrylate backbone. This compound is a trans-acid, which means that the two fluorine atoms are located on opposite sides of the double bond. The presence of the difluorophenyl group imparts unique properties to the compound, making it suitable for various applications.
What are the potential applications of (2E)-3-(2,5-Difluorophenyl)acrylic acid, trans-3-(2,5-Difluorophenyl)prop-2-enoic acid?
Due to its unique chemical structure, (2E)-3-(2,5-Difluorophenyl)acrylic acid has several potential applications. It can be used as a building block in organic synthesis to create more complex molecules. The presence of the difluorophenyl group can also impart specific properties to materials, making it useful in the development of new materials with tailored characteristics. Additionally, this compound can be utilized in the pharmaceutical industry for the synthesis of drug candidates with enhanced properties.
What sets (2E)-3-(2,5-Difluorophenyl)acrylic acid apart from other similar compounds?
One of the key distinguishing features of (2E)-3-(2,5-Difluorophenyl)acrylic acid is the presence of the difluorophenyl group on the acrylate backbone. This unique substitution pattern gives the compound distinct electronic and steric properties, which can be advantageous for specific applications. Additionally, the trans-configuration of the double bond in (2E)-3-(2,5-Difluorophenyl)acrylic acid further contributes to its unique reactivity profile compared to other isomeric forms.
How is (2E)-3-(2,5-Difluorophenyl)acrylic acid synthesized?
The synthesis of (2E)-3-(2,5-Difluorophenyl)acrylic acid typically involves starting from commercially available precursors and conducting a series of chemical reactions to introduce the difluorophenyl group onto the acrylate backbone. One common method involves the reaction of a suitable acrylate derivative with a difluorophenyl-containing reagent under specific conditions to afford the desired product. The synthetic route may vary depending on the specific starting materials and desired final product properties.
Are there any safety concerns associated with handling (2E)-3-(2,5-Difluorophenyl)acrylic acid?
As with any chemical compound, it is essential to follow proper safety protocols when handling (2E)-3-(2,5-Difluorophenyl)acrylic acid. This compound should be stored in a well-ventilated area and handled with appropriate personal protective equipment to minimize exposure. Additionally, it is crucial to be aware of the compound's potential hazards and follow recommended handling procedures to ensure safe usage.
What are some potential research directions involving (2E)-3-(2,5-Difluorophenyl)acrylic acid?
There are several exciting research directions that could be pursued using (2E)-3-(2,5-Difluorophenyl)acrylic acid. One potential avenue is the exploration of its reactivity in various chemical transformations to access new molecules with unique properties. Another area of interest could involve studying the compound's application in materials science to develop novel materials with tailored characteristics. Additionally, the synthesis of new pharmaceutical candidates based on (2E)-3-(2,5-Difluorophenyl)acrylic acid could lead to the discovery of compounds with improved biological activities.
What are the advantages of incorporating (2E)-3-(2,5-Difluorophenyl)acrylic acid into research projects or industrial applications?
The incorporation of (2E)-3-(2,5-Difluorophenyl)acrylic acid into research projects or industrial applications offers several advantages. This compound's unique chemical structure can provide access to novel molecules that may exhibit enhanced properties compared to existing compounds. Its versatility in organic synthesis makes it a valuable building block for creating more complex molecules with tailored functionalities. Additionally, the potential applications of (2E)-3-(2,5-Difluorophenyl)acrylic acid in various industries highlight its potential as a versatile and valuable compound for research and development.
How does the difluorophenyl substitution impact the properties of (2E)-3-(2,5-Difluorophenyl)acrylic acid?
The difluorophenyl substitution in (2E)-3-(2,5-Difluorophenyl)acrylic acid plays a crucial role in determining the compound's properties. Fluorine atoms are known for their ability to influence the electronic and steric properties of molecules due to their high electronegativity and small size. In this case, the presence of the difluorophenyl group can enhance the compound's stability, reactivity, and other characteristics, making it suitable for specific applications. The unique effects of fluorine substitution on the acrylate backbone contribute to the overall properties of (2E)-3-(2,5-Difluorophenyl)acrylic acid and distinguish it from other compounds.