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Structure of 1373338-09-0
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[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde features a rigid heteroaromatic core fused with an aldehyde functionality, enabling direct incorporation into conjugation workflows. This electron-deficient scaffold supports efficient transition-metal-catalyzed coupling reactions and serves as a key building block in bioactive molecule design.
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocyclic scaffolds. Its aldehyde functionality facilitates nucleophilic additions, reductive aminations, and condensation reactions under mild conditions, while the fused triazolopyridine core offers enhanced metabolic stability and favorable binding interactions. The compound exhibits excellent bench stability and compatibility with common functional groups, supporting scalable synthesis and purification via standard chromatographic methods.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: