(E)-ethyl 3-(benzyloxy)acrylate CAS:168846-45-5
(E)-Ethyl 3-(benzyloxy)acrylate finds widespread application in organic synthesis, serving as a key building block for the preparation of complex molecules. Chemists utilize its acrylate functionality for Michael addition reactions, Diels-Alder cycloadditions, and cross-coupling reactions, enabling the formation of diverse carbon-carbon and carbon-heteroatom bonds. Additionally, its benzyloxy group serves as a versatile protecting group, allowing for controlled manipulation of functional groups during synthetic pathways. In polymer chemistry, this compound acts as a monomer for the synthesis of functionalized polymers and copolymers with tailored properties. Its incorporation into polymer chains imparts desirable characteristics such as flexibility, solubility, and reactivity, making it valuable in the production of coatings, adhesives, and materials for biomedical applications. Furthermore, (E)-Ethyl 3-(benzyloxy)acrylate serves as a valuable substrate in asymmetric catalysis, enabling the synthesis of chiral molecules with high enantiomeric purity. Its use in asymmetric transformations, such as Michael additions and aldol reactions, facilitates the efficient synthesis of chiral building blocks and pharmaceutical intermediates. Overall, (E)-Ethyl 3-(benzyloxy)acrylate stands as a versatile compound in organic synthesis, offering a wide range of applications in the preparation of complex molecules, functional materials, and chiral compounds essential for various industries and research endeavors.
Composition | C12H14O3 |
Assay | 99% |
Appearance | white powder |
CAS No. | 168846-45-5 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |