In the vast universe of chemical compounds, certain molecules serve as foundational elements, enabling the creation of countless sophisticated products. 3-Bromo-4-Chloro-Benzaldehyde, identified by its unique CAS number 86265-88-5, is one such compound. This halogenated aromatic aldehyde is a pivotal intermediate, widely recognized for its utility in organic synthesis, particularly within the pharmaceutical sector. This article explores the significance of this compound, its properties, and its essential role in driving chemical innovation.

The importance of 3-Bromo-4-Chloro-Benzaldehyde stems from its molecular architecture. Featuring a benzaldehyde core substituted with both a bromine and a chlorine atom, it offers a rich platform for chemical reactions. The aldehyde functional group is highly reactive, susceptible to nucleophilic additions and condensation reactions, while the aryl halides are prime candidates for transition-metal-catalyzed cross-coupling reactions. This dual reactivity makes it an exceptionally versatile chemical building block. Researchers often seek to buy 3-Bromo-4-Chloro-Benzaldehyde to leverage these properties for synthesizing complex molecules with targeted functionalities.

In the pharmaceutical industry, CAS 86265-88-5 plays a critical role as a pharmaceutical intermediate. Its structured halogenation pattern can be instrumental in conferring specific biological activities to drug molecules. Medicinal chemists utilize it to construct novel APIs, fine-tuning molecular structures to achieve desired therapeutic effects, such as enhanced potency or improved selectivity. The consistent demand for high-purity 3-Bromo-4-Chloro-Benzaldehyde, typically above 99%, underscores its importance in the rigorous process of drug development, where purity directly impacts the efficacy and safety of the final product.

The chemical properties of 3-Bromo-4-Chloro-Benzaldehyde are well-documented. It typically appears as a white to light yellow powder, with a melting point around 70°C and a boiling point nearing 277.8°C. These physical characteristics, coupled with its molecular formula C7H4BrClO, define its handling and reaction parameters. The compound's utility extends to laboratory research, where its predictable reactivity facilitates the exploration of new synthetic routes and the development of innovative chemical processes. The extensive literature on 3-bromo-4-chloro-benzaldehyde uses highlights its adaptability across various scientific disciplines.

For manufacturers and researchers, sourcing high-quality 3-Bromo-4-Chloro-Benzaldehyde is crucial. Companies like NINGBO INNO PHARMCHEM CO.,LTD. are dedicated to providing this essential intermediate, ensuring reliable availability and adherence to strict quality standards. By supplying such critical components, they empower advancements in drug discovery, materials science, and other sectors reliant on sophisticated organic synthesis. The ongoing research into its capabilities ensures that the 3-bromo-4-chloro-benzaldehyde synthesis and application landscape will continue to expand.

In summary, 3-Bromo-4-Chloro-Benzaldehyde (CAS: 86265-88-5) is far more than just another chemical compound; it is a vital enabler of innovation. Its role as a versatile chemical building block, particularly in pharmaceutical synthesis, highlights its indispensable nature in the modern chemical industry. The continued exploration of its potential promises further advancements in scientific discovery and product development.