| Chemical Name: | 4-methyl-2-pyridin-4-yl-1,3-thiazole-5-carbaldehyde |
| CAS Number: | 892502-19-1 |
| Product Number: | AG0041V0(AGN-PC-04G0MP) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C10H8N2OS |
| Molecular Weight: | 204.2483 |
4-Methyl-2-(pyridin-4-yl)thiazole-5-carbaldehyde, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity.One of the primary applications of $name$ in chemical synthesis is as a starting material for the synthesis of various heterocyclic compounds. Its thiazole ring and pyridine moiety can undergo a range of functionalization reactions, allowing for the introduction of different substituents and modifications to tailor the properties of the final product. These structural features make $name$ a valuable tool for the construction of complex molecular architectures with specific functionalities.Moreover, the presence of the aldehyde group in $name$ enables it to participate in various condensation reactions, such as the classic aldol condensation or Knoevenagel condensation, to form carbon-carbon or carbon-nitrogen bonds. This reactivity broadens the scope of synthetic pathways that can be accessed using $name$ as a key synthetic intermediate.Overall, the strategic positioning of functional groups in 4-Methyl-2-(pyridin-4-yl)thiazole-5-carbaldehyde makes it a versatile and indispensable compound in the toolbox of synthetic chemists for the efficient construction of diverse organic molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.
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