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Structure of 1677-81-2
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3-Chloro-4-methoxypyridazine is a heterocyclic building block featuring a chlorine substituent at the 3-position and a methoxy group at the 4-position, enabling selective functionalization in medicinal chemistry. This electron-deficient pyridazine core facilitates coupling reactions under mild conditions, offering high reactivity in cross-coupling and nucleophilic substitution processes. The molecule exhibits excellent stability under standard bench conditions and demonstrates favorable solubility in common organic solvents, streamlining integration into multi-step synthetic sequences.
3-Chloro-4-methoxypyridazine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive C–Cl bond. The methoxy group enhances solubility and modulates electronic properties, while the pyridazine core provides a stable, heteroaromatic scaffold for constructing bioactive molecules. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient synthesis of complex 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: