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Structure of 37444-46-5
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Pyridazin-3-ylmethanol delivers a reactive hydroxymethyl handle at the 3-position of a pyridazine core, enabling direct functionalization in synthetic sequences. This bench-stable, moisture-tolerant scaffold integrates readily into bioactive molecule design and serves as a key intermediate for pharmaceutical and agrochemical development.
Pyridazin-3-ylmethanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through functionalization at the benzylic position. Its bench-stable nature and compatibility with common coupling and oxidation reactions facilitate straightforward derivatization for target molecule synthesis. Functions as a key intermediate in the development of kinase inhibitors and other bioactive compounds.
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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: