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Structure of 1805020-37-4
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5-Bromo-4-methoxynicotinonitrile features a bromine substituent at the 5-position and a methoxy group at the 4-position on a nicotinonitrile core. This electron-deficient heterocycle integrates readily into cross-coupling reactions, enabling efficient construction of complex pyridine-based architectures in medicinal chemistry and materials science.
5-Bromo-4-methoxynicotinonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo and nitrile functionalities. The methoxy group enhances solubility and modulates electronic properties, while the nitrile supports downstream transformations such as hydrolysis or amidation. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of heterocyclic scaffolds and functionalized aryl 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: