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Structure of 100114-58-7
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(4-Aminopyridin-2-yl)methanol features a pyridine ring bearing both an amino group at the 4-position and a hydroxymethyl substituent at the 2-position, delivering a bifunctional scaffold with enhanced solubility and synthetic versatility. This bench-stable compound integrates readily into medicinal chemistry campaigns requiring polar, nitrogen-rich motifs for target engagement or derivatization.
(4-Aminopyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. Its dual functionality—primary amine and primary alcohol—facilitates diverse transformations including amidation, etherification, and cyclization reactions. The compound exhibits good bench stability and is compatible with standard protection/deprotection sequences, making it well-suited for multi-step synthesis and API development workflows.
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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: