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Structure of 885459-73-4
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N-(3-Formylphenyl)-4-methoxybenzamide features a formyl group ortho to the amide linkage, enabling direct conjugation or cyclization in synthetic routes. The para-methoxy substituent enhances electron density and solubility. This bifunctional scaffold integrates readily into bioactive molecule frameworks under standard conditions.
N-(3-Formylphenyl)-4-methoxybenzamide serves as a versatile bifunctional building block for the synthesis of heterocyclic scaffolds and medicinal chemistry libraries. The aldehyde group enables efficient imine formation and reductive amination, while the amide functionality provides stability and compatibility with diverse reaction conditions. Its bench-stable nature and orthogonal reactivity facilitate straightforward purification and integration into multi-step synthetic sequences.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: