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Structure of 1142943-96-1
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N-(5-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide features a rigid, electron-deficient triazolopyridine core paired with a sterically constrained cyclopropylcarboxamide group. This combination imparts enhanced metabolic stability and favorable binding geometry for targeted covalent inhibition in kinase-directed drug discovery.
N-(5-Bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide serves as a versatile building block for constructing bioactive heterocycles, leveraging the bromo-substituted triazolopyridine core for palladium-catalyzed cross-coupling reactions. The cyclopropanecarboxamide moiety provides structural rigidity and favorable pharmacophoric properties, while the amide functionality offers stability and compatibility with diverse synthetic transformations. This compound exhibits bench stability and facilitates efficient purification, making it well-suited for medicinal chemistry campaigns 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: