Interesting facts
Interesting Facts about Isopropyl 3-methylbut-2-enoate
Isopropyl 3-methylbut-2-enoate is fascinating both in its structure and its applications. Here are some intriguing aspects of this compound:
- Common Uses: This compound is predominantly utilized in the synthesis of various esters and can be found in the formulation of flavors and fragrances due to its pleasant scent.
- Aromatic Properties: Isopropyl 3-methylbut-2-enoate contributes delightful fruity notes, often resulting in a sweet aroma reminiscent of tropical fruits.
- Versatile Intermediate: In the realm of organic chemistry, it serves as a valuable intermediate in reactions, aiding in the synthesis of more complex molecules.
- Applications in Polymers: The unique properties of this compound make it a potential candidate in the production of polymers, enhancing the performance characteristics of the final material.
- Safety Considerations: Like many organic compounds, handling this substance requires adherence to safety protocols to minimize exposure risks, underscoring the importance of responsible research and development practices.
As a chemist, you may find yourself captivated by the nuances of isopropyl 3-methylbut-2-enoate, whether you are working in a laboratory, studying its reactions, or exploring its myriad applications in daily life. The interplay between its structure and function showcases the beauty of organic chemistry.
Synonyms
Isopropyl 3-methyl-2-butenoate
SCHEMBL1532529
QQVQBUXUAZCLLZ-UHFFFAOYSA-N
AKOS017265435
3-Methyl,2-butenoic acid, isopropyl ester
Crotonic acid, 3-methyl-, isopropyl ester
2-Butenoic acid, 3-methyl, 1-methylethyl ester
Q27260780
Solubility of Isopropyl 3-methylbut-2-enoate
Isopropyl 3-methylbut-2-enoate, also known by its IUPAC name, exhibits interesting solubility characteristics due to its molecular structure. This compound is classified as an ester, and esters are known for their diverse solubility profiles. Here are some key points regarding its solubility:
In summary, the solubility of isopropyl 3-methylbut-2-enoate is dictated by its ester nature and molecular interactions, making it best suited for use in organic solvents rather than aqueous environments. It embodies the general trend of esters being more soluble in organic mediums compared to water.