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Structure of 1268520-74-6
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4-Chloropyrazolo[1,5-a]pyridine-7-carbonitrile features a fused heterocyclic core with complementary electron-withdrawing groups: a chlorine atom at the 4-position and a nitrile function at the 7-position. This combination enhances electrophilicity and facilitates coupling reactions in medicinal chemistry applications. The scaffold exhibits excellent stability under standard bench conditions and integrates readily into bioactive molecule architectures.
4-Chloropyrazolo[1,5-a]pyridine-7-carbonitrile serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its chloro and cyano groups enable directed metalation, Suzuki-Miyaura coupling, and nucleophilic substitution, facilitating the construction of complex pyrazolopyridine scaffolds. The molecule exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for scalable synthesis and library generation in drug discovery workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: