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Structure of 25957-65-7
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6-Azaindole-3-carboxaldehyde features a nitrogen-substituted indole core paired with an aldehyde handle at the 3-position, enabling direct incorporation into bioconjugation workflows. The electron-deficient heterocycle enhances reactivity in nucleophilic addition reactions, while the bench-stable aldehyde group tolerates standard handling protocols. This scaffold serves as a key building block for targeted probe synthesis and medicinal chemistry campaigns.
6-Azaindole-3-carboxaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of indole-based scaffolds through standard condensation and coupling reactions. The aldehyde functionality facilitates direct functionalization and acts as a key handle in iterative synthesis workflows. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for medicinal chemistry campaigns and process 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-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: