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Structure of 929568-19-4
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2-Amino-1-Boc-imidazole serves as a protected imidazole scaffold for synthetic applications, offering enhanced stability and compatibility in multi-step organic transformations. The Boc group enables selective deprotection under mild acidic conditions, facilitating downstream functionalization. This derivative integrates efficiently into heterocyclic frameworks requiring nitrogen-rich, electron-donating moieties with controlled reactivity.
2-Amino-1-Boc-imidazole serves as a versatile building block in medicinal chemistry, enabling efficient access to imidazole-containing scaffolds. The Boc group provides stability and ease of removal under mild acidic conditions, while the amino functionality supports diverse transformations including alkylation, acylation, and coupling reactions. Its compatibility with standard peptide and heterocyclic synthesis protocols makes it a practical choice for constructing bioactive molecules and functional 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: