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Structure of 1229457-94-6
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4-(4-Iodo-1H-pyrazol-1-yl)piperidine features a pyrazole ring bearing a reactive iodine substituent, enabling efficient cross-coupling transformations. The piperidine moiety provides a basic, lipophilic scaffold ideal for medicinal chemistry applications. This compound serves as a versatile building block in the synthesis of bioactive molecules and functional materials.
4-(4-Iodo-1H-pyrazol-1-yl)piperidine serves as a versatile building block for constructing bioactive heterocycles, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The iodopyrazole moiety exhibits excellent stability under standard synthetic conditions and facilitates modular assembly of complex scaffolds. Its compatibility with diverse reaction partners and ease of purification make it well-suited for medicinal chemistry campaigns and process development in API synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H301-H317-H318
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P338-P362-P405-P501
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Lot numbers can be found on the outside label of a product: