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Structure of 149805-92-5
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6-(Dimethylamino)nicotinaldehyde features a pyridine ring bearing an electron-rich dimethylamino group and a reactive aldehyde at the 6-position. This combination enables selective conjugation in bioconjugation workflows and facilitates incorporation into fluorescent probes. The compound exhibits enhanced solubility and stability under standard bench conditions, supporting efficient synthesis and handling in medicinal chemistry applications.
6-(Dimethylamino)nicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyridine-based scaffolds through condensation and coupling reactions. Its aldehyde functionality facilitates efficient derivatization, while the dimethylamino group enhances electron density at the pyridine ring, promoting reactivity in nucleophilic additions and transition-metal-catalyzed transformations. The compound exhibits bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthesis workflows in API 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: