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Structure of 102074-19-1
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5-Methyl-3-pyridinemethanol features a pyridine ring bearing a methyl group at the 5-position and a primary alcohol at the 3-position, offering a versatile scaffold for medicinal chemistry. The electron-rich aromatic core enables efficient functionalization, while the benzylic alcohol facilitates derivatization under mild conditions. This bench-stable compound integrates readily into complex molecular architectures requiring polar, heteroaromatic motifs with controlled solubility and metabolic stability.
5-Methyl-3-pyridinemethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds. Its benzyl-like reactivity facilitates straightforward functionalization at the methylene group, while the 5-methyl substituent enhances metabolic stability and modulates electronic properties. The compound exhibits excellent bench stability and compatibility with standard coupling and oxidation protocols, making it well-suited for both small-molecule synthesis and API intermediate development.
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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: