| Chemical Name: | Ethanone, 1-(2-amino-4-methyl-5-thiazolyl)-2-bromo- |
| CAS Number: | 32519-72-5 |
| Product Number: | AG00COBN(AGN-PC-02TDEI) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C6H7BrN2OS |
| Molecular Weight: | 235.10158 |
1-(2-Amino-4-methylthiazol-5-yl)-2-bromoethanone is a versatile chemical compound that finds significant application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of both bromine and thiazole functionalities into target molecules, enabling the synthesis of complex organic compounds with enhanced biological activity or specific properties.In chemical synthesis, 1-(2-Amino-4-methylthiazol-5-yl)-2-bromoethanone acts as a valuable reagent for the formation of carbon-carbon and carbon-heteroatom bonds through a variety of reactions such as nucleophilic substitution, cross-coupling, and cyclization reactions. Its bromoethanone moiety serves as an electrophilic center, facilitating the attachment of diverse functional groups to the thiazole ring, leading to the generation of structurally diverse compounds.Moreover, the presence of the amino group in the thiazole ring provides the potential for further derivatization, enabling the introduction of additional substituents for fine-tuning the properties of the synthesized molecules. Overall, 1-(2-Amino-4-methylthiazol-5-yl)-2-bromoethanone's role in chemical synthesis extends beyond mere structural incorporation, as it actively contributes to the strategic design and construction of novel compounds with tailored applications.
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