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Structure of 1060801-39-9
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3-Bromo-N,N-dimethylpyridin-2-amine features a pyridine core bearing a bromo substituent at the 3-position and a dimethylamino group at the 2-position. This configuration imparts enhanced electrophilic reactivity and improved solubility in polar organic solvents, facilitating its use in cross-coupling reactions and transition-metal-catalyzed transformations. The molecule exhibits bench-stable handling characteristics under standard conditions.
3-Bromo-N,N-dimethylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity. The bromine substituent facilitates efficient C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the dimethylamino group enhances solubility and provides a handle for further functionalization. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds 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: