3-(Thiophen-2-yl)prop-2-ynoicacid
97%
science Other reagents with same CAS 4843-44-1
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The thiophene ring enhances electronic properties, useful in materials science for developing conductive polymers or organic semiconductors. Also employed in the synthesis of heterocyclic compounds due to its reactive carboxylic acid group, which can be easily modified to esters, amides, or other derivatives for further transformations.
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