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Structure of 4603-59-2
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3,6-Dimethoxypyridazine is a bench-stable, electron-deficient heterocycle featuring two methoxy groups at the 3- and 6-positions. This substitution pattern enhances solubility in polar organic solvents while maintaining reactivity for cross-coupling and nucleophilic displacement reactions. The molecule serves as a key scaffold in medicinal chemistry and agrochemical development.
3,6-Dimethoxypyridazine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazine scaffolds via cross-coupling and nucleophilic displacement reactions. Its methoxy groups enhance solubility and provide orthogonal reactivity for sequential functionalization. The compound exhibits excellent bench stability and facilitates purification by standard chromatographic methods, making it well-suited for high-throughput synthesis and API intermediate development.
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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: