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Structure of 935-13-7
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This furan-containing carboxylic acid integrates a conjugated heterocyclic moiety with a flexible aliphatic chain, enabling efficient incorporation into bioactive scaffolds. The para-substituted furan ring enhances electron delocalization, while the pendant acid group facilitates derivatization under standard coupling conditions.
3-(Furan-2-yl)propanoic acid serves as a versatile building block for heterocyclic synthesis and bioactive molecule development. Its conjugated furan–alkyl chain enables efficient Michael additions, electrophilic substitutions, and transition-metal-catalyzed couplings. The carboxylic acid functionality offers direct access to esters, amides, and acyl chlorides, facilitating downstream derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in standard organic transformations and is well-suited for medicinal chemistry lead optimization.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: