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Structure of 1632-74-2
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3,6-Dimethylpyridazine is a sterically hindered, bench-stable heterocycle featuring two methyl groups at the 3- and 6-positions. This substitution pattern enhances electron density at the ring nitrogen atoms, facilitating selective functionalization in transition-metal-catalyzed cross-coupling reactions. The molecule serves as a robust scaffold for bioactive compound synthesis and materials chemistry applications.
3,6-Dimethylpyridazine serves as a versatile heterocyclic building block in medicinal chemistry and agrochemical synthesis. Its electron-deficient pyridazine core enables reliable coupling reactions and functionalization at C3 and C6 positions. The methyl groups enhance bench stability and improve solubility in common organic solvents, facilitating straightforward purification and scalability in multi-step syntheses.
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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: