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Structure of 1261759-41-4
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2-Chloro-5-formylbenzonitrile features a formyl group at the 5-position and a nitrile moiety at the 1-position, flanked by a chlorine substituent at the 2-position. This electron-deficient aromatic scaffold integrates readily into coupling reactions, enabling efficient access to functionalized heterocycles under mild conditions. The compound exhibits enhanced stability and solubility in common organic solvents, facilitating use in multistep synthetic sequences.
2-Chloro-5-formylbenzonitrile serves as a versatile bifunctional building block in medicinal chemistry and materials science. The formyl group enables direct functionalization via nucleophilic addition or oxime formation, while the nitrile supports reductive amination or hydrolysis to carboxamide derivatives. Its chloro substituent facilitates palladium-catalyzed cross-coupling reactions, enabling rapid access to complex heterocyclic scaffolds. The compound exhibits good bench stability and is readily purified by silica gel chromatography, supporting efficient integration into multi-step syntheses.
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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: