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Structure of 34956-29-1
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This 2-(3-formylphenyl)acetic acid features a benzene ring bearing both aldehyde and carboxylic acid functionalities in a meta relationship, enabling dual reactivity for conjugation or cyclization. The ortho-acid group enhances electrophilicity at the formyl carbon, facilitating nucleophilic addition under mild conditions. Bench-stable and moisture-tolerant, this compound serves as a key building block for bioconjugates, heterocyclic synthesis, and functionalized materials.
2-(3-Formylphenyl)acetic acid serves as a versatile bifunctional building block for the synthesis of heterocyclic scaffolds and bioactive molecules. The ortho-formyl and acetic acid groups enable sequential transformations, including condensation reactions, cyclizations, and derivatization under mild conditions. Its bench-stable nature and compatibility with common functional group manipulations make it well-suited for medicinal chemistry and process development workflows.
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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: