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Structure of 89532-79-6
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(6-Methoxypyridazin-3-yl)methanol features a pyridazine core functionalized with a methoxy group at the 6-position and a primary alcohol at the 3-position. This combination imparts enhanced solubility and metabolic stability, enabling direct incorporation into bioactive scaffolds. The pendant hydroxymethyl moiety facilitates further derivatization via esterification or ether formation, streamlining access to diverse compound libraries in medicinal chemistry.
(6-Methoxypyridazin-3-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridazinyl-containing scaffolds. Its benzylic alcohol functionality facilitates derivatization via oxidation, etherification, or esterification, while the 6-methoxy group enhances solubility and modulates electronic properties. The molecule exhibits good bench stability and compatibility with standard coupling reactions, making it suitable for use in parallel synthesis and fragment-based drug discovery campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: