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Structure of 107228-51-3
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3,6-Dichloro-4-isopropylpyridazine is a halogenated pyridazine derivative featuring two chlorine substituents at positions 3 and 6, flanked by an isopropyl group at the 4-position. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, enabling direct functionalization via cross-coupling reactions. The molecule exhibits enhanced stability under standard conditions and facilitates efficient incorporation into bioactive scaffolds through its reactive halogen sites.
3,6-Dichloro-4-isopropylpyridazine serves as a versatile building block in medicinal chemistry, enabling the construction of nitrogen-containing heterocycles via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern facilitates sequential functionalization, while the isopropyl group provides steric and electronic modulation. This compound exhibits bench stability and compatibility with standard synthetic protocols, making it suitable for modular library synthesis and API intermediate development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: