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Specifications
| Appearance | Colorless to light yellow liquid |
| Purity (GC) | 85% min. |
| Identification | HNMR spectrum corresponds to standard; Major peak retention time matches standard |
| Water | 0.5% max. |
| Boiling point | 83-85°C / 13 mmHg |
Applications
(E)-Methyl 4-bromocrotonate is primarily used as a reactive intermediate in organic synthesis, pharmaceutical development, and fine chemical production. It serves as a key building block for the preparation of substituted crotonate derivatives, heterocycles, and bioactive molecules. The compound is commonly applied in reactions such as nucleophilic substitution, cross-coupling, and Michael additions, enabling the construction of complex carbon frameworks. In research laboratories, it is used to explore reaction mechanisms, optimize synthetic pathways, and develop novel compounds for medicinal chemistry and agrochemical applications. Its bromine-substituted α,β-unsaturated ester functionality allows for versatile chemical transformations, making it a valuable tool in multi-step synthesis.
Benefits
The compound offers several advantages due to its α,β-unsaturated ester and bromide functionality. The bromine atom serves as an excellent leaving group, facilitating efficient and selective substitution or cross-coupling reactions. Its conjugated double bond enhances reactivity in Michael-type additions and other nucleophilic reactions, supporting diverse synthetic applications. The compound is soluble in common organic solvents, which allows homogeneous reaction conditions and reproducible results. Additionally, its defined stereochemistry ensures predictable reactivity and selectivity in synthetic processes, contributing to high yields and consistent product quality. These properties make it a reliable intermediate for chemical research and industrial synthesis.
Conclusion
(E)-Methyl 4-bromocrotonate is a versatile intermediate widely used in organic synthesis, pharmaceuticals, and fine chemical research. Its applications in nucleophilic substitution, cross-coupling, and carbon–carbon bond formation, combined with benefits such as reactivity, solubility, and stereochemical reliability, make it an important building block for complex molecule construction. The compound continues to support efficient and reproducible synthesis of high-value chemical products.

