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Structure of 1807017-39-5
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4-Bromo-2-chloronicotinonitrile features a trifunctional pyridine core bearing bromo, chloro, and nitrile groups at distinct positions, enabling selective functionalization in cross-coupling and heterocyclic synthesis. This electron-deficient scaffold facilitates efficient palladium-catalyzed transformations under standard conditions, delivering complex intermediates with high regiocontrol.
4-Bromo-2-chloronicotinonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogenation pattern. The nitrile group provides a handle for downstream functionalization, while the ortho-chloro and meta-bromo substituents offer orthogonal reactivity for sequential transformations. This compound exhibits excellent bench stability and facilitates efficient synthesis of complex heterocyclic scaffolds found in pharmaceutical intermediates.
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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-P301+P310-P302+P352-P304+P341-P330-P363-P501
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Lot numbers can be found on the outside label of a product: