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Structure of 1186647-69-7
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This pyrazolopyridine scaffold integrates a chloro group at C4 and an iodine substituent at C3, delivering a strategically functionalized platform for transition-metal-catalyzed cross-coupling reactions. The electron-deficient heterocyclic core enables efficient diversification in medicinal chemistry and materials science applications.
4-Chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The orthogonal reactivity of the chloro and iodo groups enables sequential cross-coupling reactions under mild conditions, facilitating efficient diversification in medicinal chemistry campaigns. Bench-stable and compatible with standard Pd-catalyzed transformations, it functions as a key intermediate in the synthesis of complex pyrazolopyridine-based API candidates.
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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#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H319
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: