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Structure of 1065099-78-6
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Ethyl 2-amino-5-methyl-1,3-oxazole-4-carboxylate features a conjugated oxazole core with complementary amino and methyl substituents, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative integrates readily in transition-metal-catalyzed coupling reactions and serves as a key intermediate for bioactive compound synthesis.
Ethyl 2-amino-5-methyl-1,3-oxazole-4-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and synthetic organic applications. Its amino and ester functionalities enable straightforward derivatization via acylation, alkylation, and coupling reactions. The oxazole core exhibits good bench stability and facilitates efficient incorporation into bioactive scaffolds, particularly in kinase inhibitor and antiviral agent development. Functional group tolerance supports multi-step synthesis with minimal protection requirements.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: