| Chemical Name: | methyl 5-amino-4-methylthiophene-2-carboxylate |
| CAS Number: | 1023655-30-2 |
| Product Number: | AG01B9XJ(AG01B9XJ) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C7H9NO2S |
| Molecular Weight: | 171.2169 |
Methyl 5-Amino-4-methylthiophene-2-carboxylate is a versatile chemical compound that finds wide applications in chemical synthesis processes. This compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials due to its unique structure and reactivity. In chemical synthesis, Methyl 5-Amino-4-methylthiophene-2-carboxylate can be used as a key intermediate in the production of heterocyclic compounds, which are essential in drug discovery and development. Its incorporation into organic molecules can lead to the creation of novel structures with potentially valuable biological activities. Furthermore, the presence of both amino and ester functional groups in Methyl 5-Amino-4-methylthiophene-2-carboxylate enables diverse synthetic pathways, allowing for the attachment of different substituents to tailor the compound for specific applications. By manipulating these functional groups, chemists can achieve precise control over the properties and reactivity of the final products, making this compound a valuable tool in organic synthesis. Overall, Methyl 5-Amino-4-methylthiophene-2-carboxylate plays a crucial role in advancing chemical synthesis strategies by offering a versatile platform for creating complex molecules with potential pharmacological, agricultural, and material science applications.
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