Interesting facts
Interesting Facts about Isopropyl 3-phenylprop-2-enoate
Isopropyl 3-phenylprop-2-enoate, a fascinating compound in the realm of organic chemistry, is notable for its unique structural characteristics and applications. Here's a closer look:
- Structure Overview: This compound features a prop-2-enoate moiety, where the carboxylate group is substituted with an isopropyl group, and a phenyl group is attached at the α-carbon. The result is a compound with intriguing properties stemming from its conjugated system.
- Chemical Reactivity: The presence of both an alkene and an ester group in its structure makes isopropyl 3-phenylprop-2-enoate a valuable participant in various chemical reactions. It is often used in organic synthesis strategies, including Michael addition and Diels-Alder reactions, due to its ability to react with nucleophiles.
- Biological Significance: Like many esters, this compound can exhibit aromatic properties that contribute to various biological activities. Its derivatives might have potential therapeutic effects, drawing interest for further research in medicinal chemistry.
- Applications in Synthesis: Isopropyl 3-phenylprop-2-enoate is often utilized as an intermediate in developing fragrances and flavoring agents. The unique aromatic profile derived from the phenyl group enhances its utility in creating complex organic molecules.
- Aromaticity and Stability: The compound's conjugated double bond configuration allows it to maintain stability and resonance, leading to interesting optical properties that scientists are exploring, particularly in the field of material science.
In conclusion, isopropyl 3-phenylprop-2-enoate serves as a prime example of how intricate organic compounds inspire innovation in chemical synthesis and applications. As noted chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas," and this compound indeed embodies the spirit of exploration in the world of chemistry!
Synonyms
Cinnamic Acid Isopropyl Ester
propan-2-yl 3-phenylprop-2-enoate
Isopropylcinnamate
RGACABDFLVLVCT-UHFFFAOYSA-N
AKOS017265329
SB66426
DB-002762
C1779
Solubility of Isopropyl 3-phenylprop-2-enoate
Isopropyl 3-phenylprop-2-enoate, with the chemical formula C12H14O, exhibits interesting solubility properties that play a crucial role in its applications. Understanding its solubility can provide insights into how it behaves in various environments.
As a general rule in solubility, "like dissolves like," meaning that polar solvents are better for polar solutes and non-polar solvents are more effective for non-polar solutes. Thus, the limited water solubility of isopropyl 3-phenylprop-2-enoate makes it an ideal candidate for organic reactions and formulations where non-polar environments are prevalent.
In summary, isopropyl 3-phenylprop-2-enoate is a compound with unique solubility characteristics primarily favorable in organic media, making it valuable for various chemical synthesis processes.