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Structure of 22433-90-5
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2-Bromoisophthalonitrile features a rigid, electron-deficient aromatic core with strategically positioned bromine and nitrile groups. This combination enables direct functionalization in cross-coupling reactions and facilitates integration into heterocyclic scaffolds. The molecule exhibits excellent stability under standard conditions, supporting reliable use in synthetic workflows requiring precise substitution patterns.
2-Bromoisophthalonitrile serves as a versatile building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds through palladium-catalyzed cross-coupling reactions. Its dual nitrile and bromide functionalities offer orthogonal reactivity, facilitating sequential transformations with high chemoselectivity. The compound exhibits excellent bench stability and is compatible with standard reaction conditions, making it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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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-H332-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: