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Structure of 1250628-49-9
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N-Ethyl-6-methylpyridazin-3-amine features a pyridazin-3-amine core with complementary ethyl and methyl substituents that enhance solubility and modulate electronic properties. This bench-stable heterocycle integrates readily into medicinal chemistry scaffolds, offering a robust platform for targeted molecular design in kinase inhibitor development and functionalized small molecule synthesis.
N-Ethyl-6-methylpyridazin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridazinone-based scaffolds through standard functionalization protocols. Its electron-rich heterocyclic core exhibits favorable stability and solubility, facilitating downstream derivatization via nucleophilic substitution or transition-metal-catalyzed coupling. The presence of both alkylated nitrogen and methyl substituents enhances regioselectivity in synthetic transformations, making it a practical choice for constructing bioactive molecules in drug discovery campaigns.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H315-H318-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: