AD78170
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $132.00 | $93.00 | - + | |
250mg | 98% | in stock | $210.00 | $147.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AD78170 |
Chemical Name: | 8-(Trifluoromethyl)quinolin-6-amine |
CAS Number: | 1080640-91-0 |
Molecular Formula: | C10H7F3N2 |
Molecular Weight: | 212.1712 |
MDL Number: | MFCD11052592 |
SMILES: | Nc1cc2cccnc2c(c1)C(F)(F)F |
8-(Trifluoromethyl)quinolin-6-amine, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and structural properties. In the realm of organic chemistry, it serves as a valuable building block for the creation of various functional molecules and pharmaceutical intermediates. Its trifluoromethyl group imparts enhanced hydrophobicity and electron-withdrawing capabilities, making it advantageous for the modification of organic substrates.One of the key applications of 8-(Trifluoromethyl)quinolin-6-amine is in the synthesis of bioactive compounds and drug candidates. By strategically incorporating this compound into synthetic routes, chemists can introduce desirable physicochemical properties and biological activities into target molecules. Additionally, the presence of the quinoline scaffold further enhances the potential of $name$ in medicinal chemistry, as quinoline derivatives have demonstrated diverse pharmacological profiles, ranging from antimicrobial to anticancer activities.Moreover, the unique reactivity of 8-(Trifluoromethyl)quinolin-6-amine allows for the formation of complex molecular architectures through various functional group transformations. Its compatibility with a wide range of synthetic methodologies, including cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations, enables chemists to access structurally diverse compounds efficiently.In summary, 8-(Trifluoromethyl)quinolin-6-amine plays a crucial role in advancing the field of chemical synthesis by offering a valuable platform for the construction of biologically active molecules and functional materials. Its versatility and reactivity make it an indispensable tool for synthetic chemists seeking to develop innovative solutions in drug discovery, material science, and beyond.