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Structure of 66947-92-0
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Methyl 2-amino-1,3-benzothiazole-6-carboxylate features a fused heterocyclic core with a strategically positioned amino group and ester functionality. This combination enables direct integration into pharmaceutical scaffolds and synthetic intermediates, offering enhanced solubility and reactivity under standard conditions. The molecule demonstrates bench-stable handling characteristics and serves as a key building block for bioactive compound development.
Methyl 2-amino-1,3-benzothiazole-6-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive benzothiazole scaffolds. Its amino and ester functionalities offer orthogonal reactivity for downstream derivatization, including amidation, coupling reactions, and heterocycle functionalization. The compound exhibits bench stability and facilitates straightforward purification, supporting scalable synthesis of potential pharmaceutical intermediates.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: