Interesting facts
Interesting Facts about 3-(2-furyl)prop-2-enal
3-(2-furyl)prop-2-enal, commonly referred to as a furyl acrylaldehyde, is a fascinating compound that bridges the worlds of organic chemistry and aromatic compounds. Here are some insightful aspects:
- Structure and Reactivity: The unique structure of 3-(2-furyl)prop-2-enal features a furyl group, which is a five-membered aromatic ring containing oxygen. This makes it an interesting candidate for electrophilic reactions.
- Applications: It has significant implications in the fields of flavoring and fragrance. The furyl moiety contributes a distinctive aroma that is often desirable in perfumery.
- Synthetic Intermediates: The compound serves as a useful intermediate in organic synthesis, aiding in the production of various pharmaceuticals and complex organic molecules.
- Biological Activity: Research has indicated potential biological activities that may be beneficial, making it a compound of interest in medicinal chemistry.
- Historical Significance: Compounds like 3-(2-furyl)prop-2-enal have been studied for many years, providing invaluable insights into the chemical behaviors of heterocyclic compounds.
Overall, 3-(2-furyl)prop-2-enal stands out for its versatility in both organic synthesis and application in the aroma industry, showcasing the beauty of chemistry in merging structure with practical use.
Synonyms
3-(2-Furanyl)-2-propenal
Furfuryliden-acetaldehyd
3-(2-furyl)-acrolein
beta-(2-FURYL)ACROLEIN
DTXSID2025349
AKOS025243212
SB60942
NCI60_001734
DB-049425
Solubility of 3-(2-furyl)prop-2-enal
3-(2-furyl)prop-2-enal, a compound with a furan ring and an aldehyde functional group, presents interesting solubility characteristics. Its solubility is influenced by several key factors:
As a result, one might say that the solubility of 3-(2-furyl)prop-2-enal in water is "limited," but it finds a better home in various organic solvents.
Quote: "In chemistry, solubility enhances the understanding of compound behavior and interaction." Thus, exploring the solubility of this compound broadens its applications in organic synthesis and reaction mechanisms.