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Structure of 56026-36-9
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Methyl 6-(hydroxymethyl)nicotinate features a pyridine ring with strategically positioned ester and hydroxymethyl groups, enabling direct incorporation into bioactive molecule scaffolds. The hydroxymethyl functionality offers a handle for selective derivatization under mild conditions, while the ester group enhances solubility and stability in organic media. This compound serves as a key building block for NAD+ analogs and related redox cofactor systems.
Methyl 6-(hydroxymethyl)nicotinate serves as a versatile building block in synthetic organic chemistry, enabling straightforward functionalization at the pyridine ring’s C6 position. The pendant hydroxymethyl group facilitates oxidation to carboxylic acid, reduction to alcohol, or ether formation, while the methyl ester supports standard transformations such as hydrolysis or coupling reactions. Its bench-stable nature and compatibility with common protecting group strategies make it a practical choice for constructing heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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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: