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Structure of 142892-31-7
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2-(3-Bromopyridin-4-yl)acetonitrile features a brominated pyridine core paired with a nitrile-bearing acetyl side chain, enabling direct incorporation into cross-coupling and cyclization workflows. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations, while the nitrile group serves as a versatile handle for downstream functionalization. This bench-stable intermediate supports efficient synthesis of bioactive heterocycles and advanced pharmaceutical intermediates.
2-(3-Bromopyridin-4-yl)acetonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo and nitrile functionalities. The acetonitrile group enhances solubility and offers a handle for further derivatization, while the pyridine scaffold provides orthogonal reactivity. Bench-stable and compatible with standard synthetic workflows, it facilitates efficient construction of heterocyclic scaffolds and API 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-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: