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Specifications
| Appearance: | Yellow to colorless liquid |
| 1H-NMR: | Conforms to reference |
| Purity (NMR): | 95.0% min |
Applications
alpha-Bromobutyric acid, (R)- is primarily used as a chiral building block in organic and medicinal chemistry. It serves as a key intermediate for the synthesis of enantiomerically pure amino acids, peptide derivatives, and other biologically active molecules. Its α-bromo functionality allows selective nucleophilic substitution to introduce various functional groups, such as amines, thiols, or alcohols, facilitating the design of target molecules with precise stereochemistry. In pharmaceutical research, it is employed for constructing drugs and enzyme inhibitors that require defined chiral centers for optimal activity. The compound is also used in agrochemical synthesis to prepare chiral intermediates for pesticides and herbicides. Additionally, it is valuable in asymmetric synthesis and chemical methodology studies, where it serves as a model substrate for developing stereoselective reactions and enantioselective transformations.
Benefits
The benefits of alpha-Bromobutyric acid, (R)- include its high enantiomeric purity, chemical reactivity, and versatility in synthesis. The defined (R)-configuration ensures that downstream products retain desired stereochemistry, which is critical for biological activity and pharmacological effectiveness. The α-bromo group allows efficient functionalization under mild conditions, reducing side reactions and improving synthetic yields. Its compatibility with a range of nucleophiles and reaction conditions makes it a flexible intermediate for diverse applications. Furthermore, its stability under standard storage and handling conditions allows reproducible results in laboratory and industrial-scale syntheses. By providing access to chiral building blocks, it facilitates the efficient production of high-value pharmaceuticals and specialty chemicals.
Conclusion
In summary, alpha-Bromobutyric acid, (R)- is a chiral α-bromo carboxylic acid widely used as a versatile intermediate in the synthesis of enantiomerically pure pharmaceuticals, agrochemicals, and biologically active molecules. Its stereochemical definition, reactivity, and synthetic flexibility make it a key component in asymmetric synthesis and medicinal chemistry, enabling precise control over molecular structure and activity in downstream applications.

