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Structure of 18617-50-0
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Ethyl 6-hydroxynicotinate features a hydroxyl group at the 6-position of the nicotinate ring, enabling direct functionalization in synthetic sequences. This bench-stable derivative integrates readily into heterocyclic scaffolds and serves as a key intermediate for bioactive molecules requiring polar, hydrogen-bonding capabilities.
Ethyl 6-hydroxynicotinate serves as a versatile building block in synthetic organic chemistry, enabling straightforward functionalization at the C6 position. The pendant hydroxyl group facilitates derivatization via esterification, ether formation, or oxidation to carboxylic acid, while the ester functionality supports standard amidation and reduction protocols. Its stability under common reaction conditions and compatibility with diverse protecting groups make it well-suited for constructing heterocyclic scaffolds and medicinal chemistry 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: