CAS · 99-40-1
Product Overview
2-Chloro-3,4-dihydroxyacetophenone is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance: | Light to dark grey powder, also with red or brown tint |
|---|---|
| Water: | 0.5% max |
| Loss on Drying: | 0.5% max |
| Purity: | 99% min |
| Single Impurity: | 0.1% max |
| Total Impurity: | 0.5% max |
| 1,2-Dichloroethane: | 50 ppm max |
Applications
2-Chloro-3,4-dihydroxyacetophenone (CAS 99-40-1) is an aromatic compound with hydroxyl and chloro substituents that make it a useful intermediate in pharmaceutical, agrochemical, and fine chemical synthesis. It is employed in the preparation of bioactive molecules, including antimicrobial, anti-inflammatory, and antioxidant agents. The compound's catechol structure enhances its reactivity, allowing it to serve as a precursor in the synthesis of heterocycles and natural product derivatives. In addition, it is used in research settings to explore structure–activity relationships of phenolic compounds, as well as in the design of functional materials and coordination complexes in materials science.
Benefits
The benefits of 2-chloro-3,4-dihydroxyacetophenone lie in its multifunctional chemical structure, which combines hydroxyl groups with a chloro-substituted aromatic ring. This combination offers high versatility in substitution, condensation, and coupling reactions, enabling the efficient synthesis of diverse compounds. Its phenolic groups provide antioxidant properties and the ability to form strong interactions with biological targets or metal ions, expanding its utility across multiple fields. The compound's reactivity allows for controlled chemical modifications, making it a valuable scaffold for designing pharmaceuticals and advanced materials.
Conclusion
2-Chloro-3,4-dihydroxyacetophenone is a versatile intermediate with important applications in drug discovery, agrochemical development, and material science. Its reactive catechol framework and chloro substituent support efficient molecular transformations and functionalization. By enabling the synthesis of bioactive compounds and advanced materials, it continues to be a valuable tool in both academic research and industrial applications.
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