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Structure of 302964-02-9
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2-Boc-Aminothiazole-5-carboxylic acid features a protected amine and carboxylic acid functional group on a thiazole scaffold, enabling direct incorporation into peptide-like architectures. The Boc group ensures stability during synthesis and facilitates selective deprotection under mild acidic conditions. This bifunctional building block supports efficient access to heterocyclic scaffolds in medicinal chemistry and materials science.
2-Boc-Aminothiazole-5-carboxylic acid serves as a versatile building block for the synthesis of thiazole-based heterocycles, enabling efficient access to medicinally relevant scaffolds. The Boc group provides stable protection of the amine under standard reaction conditions, while the carboxylic acid functionality facilitates direct coupling or derivatization. This compound exhibits excellent bench stability and compatibility with common synthetic protocols, including amide bond formation and transition-metal-catalyzed cross-couplings. Its defined reactivity profile makes it ideal for modular construction in medicinal chemistry campaigns targeting kinase inhibitors and other bioactive molecules.
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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: