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Structure of 89891-69-0
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3-Bromo-4-formylbenzonitrile features a strategically positioned formyl group adjacent to a nitrile moiety, enabling direct functionalization in cross-coupling and cyclization reactions. The bromine atom provides a reliable handle for palladium-mediated transformations, while the electron-deficient aromatic ring enhances reactivity in nucleophilic substitution processes. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced pharmaceutical scaffolds.
3-Bromo-4-formylbenzonitrile serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its bromo substituent. The formyl group facilitates nucleophilic additions and oxime formation, while the nitrile acts as a handle for hydrolysis or reduction. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for constructing complex heterocyclic scaffolds and 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-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: