| Chemical Name: | Quinoline, 3-(chloromethyl)-, hydrochloride |
| CAS Number: | 21863-56-9 |
| Product Number: | AG01B7WD(AGN-PC-001RQ4) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C10H9Cl2N |
| Molecular Weight: | 214.0912 |
3-(Chloromethyl)quinoline hydrochloride is a versatile compound frequently utilized in chemical synthesis for its reactivity and selectivity in various reactions. This compound serves as a valuable building block in the preparation of complex organic molecules due to its specific functional groups and unique structural properties.One important application of 3-(Chloromethyl)quinoline hydrochloride in chemical synthesis is its role as a key intermediate in the synthesis of pharmaceutical compounds. By incorporating this compound into the reaction sequence, chemists can introduce the quinoline ring system with a chloromethyl group in a controlled manner, allowing for further modification and elaboration to produce biologically active molecules. The presence of the chloromethyl group provides a site for selective functionalization, enabling the synthesis of diverse pharmacologically relevant structures.Furthermore, 3-(Chloromethyl)quinoline hydrochloride is commonly used in the preparation of advanced materials such as polymers, dyes, and agrochemicals. Its reactivity under various reaction conditions allows for the introduction of quinoline moieties into the final products, thereby imparting specific properties or functionalities to the materials. This compound plays a crucial role in the design and synthesis of new materials with tailored characteristics for a wide range of applications.In addition to its applications in the pharmaceutical and materials science industries, 3-(Chloromethyl)quinoline hydrochloride also finds utility in academic research settings for exploring new reaction pathways and developing novel synthetic methodologies. Its versatile reactivity makes it a valuable tool for organic chemists seeking to access complex molecular structures efficiently and selectively, contributing to advancements in the field of chemical synthesis.
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