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Structure of 293742-29-7
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4-Hydroxythiophene-2-carbaldehyde features a hydroxyl group adjacent to a reactive aldehyde on a thiophene scaffold, enabling direct conjugation and functionalization. This electron-rich heterocycle facilitates coupling reactions under mild conditions, offering stable access to bioactive thienyl architectures in medicinal chemistry and materials synthesis.
4-Hydroxythiophene-2-carbaldehyde serves as a versatile heterocyclic building block in medicinal chemistry and synthetic organic research. The molecule combines a reactive aldehyde group with a phenolic hydroxyl, enabling facile derivatization via condensation, oxidation, or cross-coupling reactions. Its structural motif is frequently encountered in bioactive scaffolds due to favorable electronic properties and metabolic stability. Bench-stable and amenable to purification by standard chromatographic methods, it functions effectively in multi-step synthesis workflows requiring orthogonality between functional groups.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: