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Structure of 941294-54-8
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5-Bromo-2-methoxynicotinonitrile features a bromine substituent at the 5-position and a methoxy group at the 2-position on a nicotinonitrile core. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key building block for functionalized pyridines in medicinal chemistry and materials science.
5-Bromo-2-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 molecule exhibits excellent bench stability and compatibility with standard synthetic protocols. It functions as a key intermediate in the construction of substituted heterocycles and bioactive scaffolds.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: